Canonical Allele Identifier: CA412799777

Gene: KDM6A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.45078507T>C , CM000685.2:g.45078507T>C	GRCh38
NC_000023.10:g.44937752T>C , CM000685.1:g.44937752T>C	GRCh37
NC_000023.9:g.44822696T>C	NCBI36
NG_016260.1:g.210330T>C , LRG_616:g.210330T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001291415.2:c.3094+2T>C MANE Select	NP_001278344.1:n.3094+2T>C
ENST00000611820.5:c.3094+2T>C MANE Select	ENSP00000483595.2:n.3094+2T>C
NM_001291415.1:c.3094+2T>C , LRG_616t1:c.3094+2T>C	NP_001278344.1:n.3094+2T>C
NM_001291416.1:c.2959+2T>C	NP_001278345.1:n.2959+2T>C
NM_001291416.2:c.2959+2T>C	NP_001278345.1:n.2959+2T>C
NM_001291417.1:c.2803+2T>C	NP_001278346.1:n.2803+2T>C
NM_001291417.2:c.2803+2T>C	NP_001278346.1:n.2803+2T>C
NM_001291418.1:c.2701+2T>C	NP_001278347.1:n.2701+2T>C
NM_001291418.2:c.2701+2T>C	NP_001278347.1:n.2701+2T>C
NM_001291421.1:c.2050+2T>C	NP_001278350.1:n.2050+2T>C
NM_001291421.2:c.2050+2T>C	NP_001278350.1:n.2050+2T>C
NM_021140.3:c.2938+2T>C	NP_066963.2:n.2938+2T>C
NM_021140.4:c.2938+2T>C	NP_066963.2:n.2938+2T>C
NR_111960.1:n.3234+2T>C
NR_111960.2:n.3221+2T>C
ENST00000377967.8:c.2938+2T>C	ENSP00000367203.4:n.2938+2T>C
ENST00000377967.9:c.2938+2T>C	ENSP00000367203.4:n.2938+2T>C
ENST00000382899.8:c.2887+2T>C	ENSP00000372355.5:n.2887+2T>C
ENST00000382899.9:c.2959+2T>C	ENSP00000372355.6:n.2959+2T>C
ENST00000414389.5:c.1730+2T>C
ENST00000433797.5:c.1865+2T>C
ENST00000536777.5:c.2731+2T>C	ENSP00000437405.2:n.2731+2T>C
ENST00000536777.6:c.2803+2T>C	ENSP00000437405.3:n.2803+2T>C
ENST00000543216.5:c.2785+2T>C	ENSP00000443078.2:n.2785+2T>C
ENST00000543216.6:c.2701+2T>C	ENSP00000443078.3:n.2701+2T>C
ENST00000611820.4:c.3022+2T>C	ENSP00000483595.1:n.3022+2T>C
ENST00000621147.4:c.2595+14T>C	ENSP00000478793.1:n.2595+14T>C
ENST00000674541.1:c.*2226+2T>C	ENSP00000501919.1:n.*2226+2T>C
ENST00000674564.1:c.2857+2T>C	ENSP00000502150.1:n.2857+2T>C
ENST00000674586.1:c.3016+2T>C	ENSP00000502660.1:n.3016+2T>C
ENST00000674659.1:c.*2382+2T>C	ENSP00000502255.1:n.*2382+2T>C
ENST00000674739.1:n.3996+2T>C
ENST00000674867.1:c.2800+2T>C	ENSP00000502060.1:n.2800+2T>C
ENST00000675157.1:n.2545+2T>C
ENST00000675182.1:n.2978+2T>C
ENST00000675440.1:n.3114+2T>C
ENST00000675514.1:c.2938+2T>C	ENSP00000502759.1:n.2938+2T>C
ENST00000675525.1:n.5060+2T>C
ENST00000675546.1:n.9644+2T>C
ENST00000675577.1:c.2836+2T>C	ENSP00000501855.1:n.2836+2T>C
ENST00000675816.1:n.3114+2T>C
ENST00000676062.1:c.2959+2T>C	ENSP00000502311.1:n.2959+2T>C
ENST00000676085.1:c.*2124+2T>C	ENSP00000501752.1:n.*2124+2T>C
ENST00000676133.1:c.*2991+2T>C	ENSP00000502586.1:n.*2991+2T>C
ENST00000676343.1:c.2959+2T>C	ENSP00000501761.1:n.2959+2T>C
ENST00000676389.1:n.3381+2T>C
ENST00000682908.1:c.2838+2T>C	ENSP00000508158.1:n.2838+2T>C
ENST00000683021.1:c.2857+2T>C	ENSP00000507416.1:n.2857+2T>C
ENST00000683425.1:c.*2421+2T>C	ENSP00000507291.1:n.*2421+2T>C
ENST00000684352.1:c.2868+2T>C	ENSP00000508379.1:n.2868+2T>C
XM_005272656.3:c.2992+2T>C	XP_005272713.1:n.2992+2T>C
XM_005272656.5:c.2992+2T>C	XP_005272713.1:n.2992+2T>C
XM_005272659.3:c.2836+2T>C	XP_005272716.1:n.2836+2T>C
XM_005272659.5:c.2836+2T>C	XP_005272716.1:n.2836+2T>C
XM_011543957.1:c.3151+2T>C	XP_011542259.1:n.3151+2T>C
XM_011543958.1:c.3094+2T>C	XP_011542260.1:n.3094+2T>C
XM_011543958.3:c.3094+2T>C	XP_011542260.1:n.3094+2T>C
XM_011543959.1:c.3049+2T>C	XP_011542261.1:n.3049+2T>C
XM_011543960.1:c.3151+2T>C	XP_011542262.1:n.3151+2T>C
XM_011543961.1:c.3016+2T>C	XP_011542263.1:n.3016+2T>C
XM_011543962.1:c.2995+2T>C	XP_011542264.1:n.2995+2T>C
XM_011543963.1:c.2959+2T>C	XP_011542265.1:n.2959+2T>C
XM_011543963.3:c.2959+2T>C	XP_011542265.1:n.2959+2T>C
XM_011543964.1:c.2938+2T>C	XP_011542266.1:n.2938+2T>C
XM_011543964.3:c.2938+2T>C	XP_011542266.1:n.2938+2T>C
XM_011543965.1:c.2914+2T>C	XP_011542267.1:n.2914+2T>C
XM_011543966.1:c.2893+2T>C	XP_011542268.1:n.2893+2T>C
XM_011543967.1:c.2995+2T>C	XP_011542269.1:n.2995+2T>C
XM_011543968.1:c.2860+2T>C	XP_011542270.1:n.2860+2T>C
XM_011543969.1:c.2857+2T>C	XP_011542271.1:n.2857+2T>C
XM_011543969.3:c.2857+2T>C	XP_011542271.1:n.2857+2T>C
XM_011543970.1:c.2836+2T>C	XP_011542272.1:n.2836+2T>C
XM_011543970.3:c.2836+2T>C	XP_011542272.1:n.2836+2T>C
XM_011543971.1:c.2914+2T>C	XP_011542273.1:n.2914+2T>C
XM_011543972.1:c.2803+2T>C	XP_011542274.1:n.2803+2T>C
XM_011543972.3:c.2803+2T>C	XP_011542274.1:n.2803+2T>C
XM_011543973.1:c.2860+2T>C	XP_011542275.1:n.2860+2T>C
XM_011543974.1:c.2938+2T>C	XP_011542276.1:n.2938+2T>C
XM_011543974.2:c.2938+2T>C	XP_011542276.1:n.2938+2T>C
XM_011543975.1:c.2341+2T>C	XP_011542277.1:n.2341+2T>C
XM_011543975.2:c.2341+2T>C	XP_011542277.1:n.2341+2T>C
XM_011543976.1:c.3151+2T>C	XP_011542278.1:n.3151+2T>C
XM_017029783.2:c.2857+2T>C	XP_016885272.1:n.2857+2T>C
XM_017029784.1:c.2206+2T>C	XP_016885273.1:n.2206+2T>C
XM_017029785.1:c.1948+2T>C	XP_016885274.1:n.1948+2T>C
XM_024452438.1:c.2992+2T>C	XP_024308206.1:n.2992+2T>C
XM_024452439.1:c.2569+2T>C	XP_024308207.1:n.2569+2T>C
XR_002958804.1:n.3464+2T>C
XR_949018.1:n.3528+2T>C