Canonical Allele Identifier: CA329050161

Gene: KDM6A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.45070001C>T , CM000685.2:g.45070001C>T	GRCh38
NC_000023.10:g.44929246C>T , CM000685.1:g.44929246C>T	GRCh37
NC_000023.9:g.44814190C>T	NCBI36
NG_016260.1:g.201824C>T , LRG_616:g.201824C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001291415.2:c.2502C>T MANE Select	NP_001278344.1:p.Ala834=
ENST00000611820.5:c.2502C>T MANE Select	ENSP00000483595.2:p.Ala834=
NM_001291415.1:c.2502C>T , LRG_616t1:c.2502C>T	NP_001278344.1:p.Ala834=
NM_001291416.1:c.2367C>T	NP_001278345.1:p.Ala789=
NM_001291416.2:c.2367C>T	NP_001278345.1:p.Ala789=
NM_001291417.1:c.2211C>T	NP_001278346.1:p.Ala737=
NM_001291417.2:c.2211C>T	NP_001278346.1:p.Ala737=
NM_001291418.1:c.2109C>T	NP_001278347.1:p.Ala703=
NM_001291418.2:c.2109C>T	NP_001278347.1:p.Ala703=
NM_001291421.1:c.1458C>T	NP_001278350.1:p.Ala486=
NM_001291421.2:c.1458C>T	NP_001278350.1:p.Ala486=
NM_021140.3:c.2346C>T	NP_066963.2:p.Ala782=
NM_021140.4:c.2346C>T	NP_066963.2:p.Ala782=
NR_111960.1:n.2642C>T
NR_111960.2:n.2629C>T
ENST00000377967.8:c.2346C>T	ENSP00000367203.4:p.Ala782=
ENST00000377967.9:c.2346C>T	ENSP00000367203.4:p.Ala782=
ENST00000382899.8:c.2295C>T	ENSP00000372355.5:p.Ala765=
ENST00000382899.9:c.2367C>T	ENSP00000372355.6:p.Ala789=
ENST00000414389.5:c.1138C>T
ENST00000433797.5:c.1273C>T
ENST00000536777.5:c.2139C>T	ENSP00000437405.2:p.Ala713=
ENST00000536777.6:c.2211C>T	ENSP00000437405.3:p.Ala737=
ENST00000543216.5:c.2193C>T	ENSP00000443078.2:p.Ala731=
ENST00000543216.6:c.2109C>T	ENSP00000443078.3:p.Ala703=
ENST00000611820.4:c.2430C>T	ENSP00000483595.1:p.Ala810=
ENST00000621147.4:c.2015C>T	ENSP00000478793.1:n.2015C>T
ENST00000621147.5:c.2015C>T	ENSP00000478793.1:n.2015C>T
ENST00000674541.1:c.*1634C>T	ENSP00000501919.1:n.*1634C>T
ENST00000674564.1:c.2265C>T	ENSP00000502150.1:p.Ala755=
ENST00000674586.1:c.2424C>T	ENSP00000502660.1:p.Ala808=
ENST00000674659.1:c.*1790C>T	ENSP00000502255.1:n.*1790C>T
ENST00000674739.1:n.3404C>T
ENST00000674867.1:c.2208C>T	ENSP00000502060.1:p.Ala736=
ENST00000675157.1:n.1953C>T
ENST00000675182.1:n.2386C>T
ENST00000675440.1:n.2522C>T
ENST00000675514.1:c.2346C>T	ENSP00000502759.1:p.Ala782=
ENST00000675525.1:n.4468C>T
ENST00000675546.1:n.2713C>T
ENST00000675577.1:c.2244C>T	ENSP00000501855.1:p.Ala748=
ENST00000675816.1:n.2522C>T
ENST00000676062.1:c.2367C>T	ENSP00000502311.1:p.Ala789=
ENST00000676085.1:c.*1532C>T	ENSP00000501752.1:n.*1532C>T
ENST00000676133.1:c.*2399C>T	ENSP00000502586.1:n.*2399C>T
ENST00000676343.1:c.2367C>T	ENSP00000501761.1:p.Ala789=
ENST00000676389.1:n.2789C>T
ENST00000682908.1:c.2246C>T	ENSP00000508158.1:n.2246C>T
ENST00000683021.1:c.2265C>T	ENSP00000507416.1:p.Ala755=
ENST00000683425.1:c.*1829C>T	ENSP00000507291.1:n.*1829C>T
ENST00000684352.1:c.2367C>T	ENSP00000508379.1:p.Ala789=
XM_005272656.3:c.2400C>T	XP_005272713.1:p.Ala800=
XM_005272656.5:c.2400C>T	XP_005272713.1:p.Ala800=
XM_005272659.3:c.2244C>T	XP_005272716.1:p.Ala748=
XM_005272659.5:c.2244C>T	XP_005272716.1:p.Ala748=
XM_011543957.1:c.2559C>T	XP_011542259.1:p.Ala853=
XM_011543958.1:c.2502C>T	XP_011542260.1:p.Ala834=
XM_011543958.3:c.2502C>T	XP_011542260.1:p.Ala834=
XM_011543959.1:c.2457C>T	XP_011542261.1:p.Ala819=
XM_011543960.1:c.2559C>T	XP_011542262.1:p.Ala853=
XM_011543961.1:c.2424C>T	XP_011542263.1:p.Ala808=
XM_011543962.1:c.2403C>T	XP_011542264.1:p.Ala801=
XM_011543963.1:c.2367C>T	XP_011542265.1:p.Ala789=
XM_011543963.3:c.2367C>T	XP_011542265.1:p.Ala789=
XM_011543964.1:c.2346C>T	XP_011542266.1:p.Ala782=
XM_011543964.3:c.2346C>T	XP_011542266.1:p.Ala782=
XM_011543965.1:c.2322C>T	XP_011542267.1:p.Ala774=
XM_011543966.1:c.2301C>T	XP_011542268.1:p.Ala767=
XM_011543967.1:c.2403C>T	XP_011542269.1:p.Ala801=
XM_011543968.1:c.2268C>T	XP_011542270.1:p.Ala756=
XM_011543969.1:c.2265C>T	XP_011542271.1:p.Ala755=
XM_011543969.3:c.2265C>T	XP_011542271.1:p.Ala755=
XM_011543970.1:c.2244C>T	XP_011542272.1:p.Ala748=
XM_011543970.3:c.2244C>T	XP_011542272.1:p.Ala748=
XM_011543971.1:c.2322C>T	XP_011542273.1:p.Ala774=
XM_011543972.1:c.2211C>T	XP_011542274.1:p.Ala737=
XM_011543972.3:c.2211C>T	XP_011542274.1:p.Ala737=
XM_011543973.1:c.2268C>T	XP_011542275.1:p.Ala756=
XM_011543974.1:c.2346C>T	XP_011542276.1:p.Ala782=
XM_011543974.2:c.2346C>T	XP_011542276.1:p.Ala782=
XM_011543975.1:c.1749C>T	XP_011542277.1:p.Ala583=
XM_011543975.2:c.1749C>T	XP_011542277.1:p.Ala583=
XM_011543976.1:c.2559C>T	XP_011542278.1:p.Ala853=
XM_017029783.2:c.2265C>T	XP_016885272.1:p.Ala755=
XM_017029784.1:c.1614C>T	XP_016885273.1:p.Ala538=
XM_017029785.1:c.1356C>T	XP_016885274.1:p.Ala452=
XM_024452438.1:c.2400C>T	XP_024308206.1:p.Ala800=
XM_024452439.1:c.1977C>T	XP_024308207.1:p.Ala659=
XR_002958804.1:n.2872C>T
XR_949018.1:n.2936C>T