Canonical Allele Identifier: CA477359426

Gene: KMT2A

Linked Data

• MyVariant Identifiers: chr11:g.118374035T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503320T>C , CM000673.2:g.118503320T>C	GRCh38
NC_000011.9:g.118374035T>C , CM000673.1:g.118374035T>C	GRCh37
NC_000011.8:g.117879245T>C	NCBI36
NG_027813.1:g.71831T>C , LRG_613:g.71831T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.7527T>C	ENSP00000432391.3:p.Tyr2509=
ENST00000710560.1:c.7518T>C	ENSP00000518343.1:p.Tyr2506=
ENST00000649878.2:c.1467T>C	ENSP00000497891.2:p.Tyr489=
ENST00000685397.1:c.1467T>C	ENSP00000509586.1:p.Tyr489=
ENST00000686370.1:c.1467T>C	ENSP00000509179.1:p.Tyr489=
ENST00000689424.1:c.1725T>C	ENSP00000509852.1:p.Tyr575=
ENST00000691053.1:c.7500T>C	ENSP00000509168.1:p.Tyr2500=
ENST00000389506.10:c.7419T>C	ENSP00000374157.5:p.Tyr2473=
ENST00000528278.2:n.6770T>C
ENST00000534358.8:c.7428T>C MANE Select	ENSP00000436786.2:p.Tyr2476=
ENST00000649699.1:c.7305T>C	ENSP00000496927.1:p.Tyr2435=
ENST00000389506.9:c.7419T>C	ENSP00000374157.5:p.Tyr2473=
ENST00000528278.1:n.1555T>C
ENST00000534358.5:c.7428T>C	ENSP00000436786.1:p.Tyr2476=
NM_001197104.1:c.7428T>C , LRG_613t1:c.7428T>C	NP_001184033.1:p.Tyr2476=
NM_005933.3:c.7419T>C	NP_005924.2:p.Tyr2473=
XM_006718839.2:c.4911T>C	XP_006718902.2:p.Tyr1637=
XM_011542829.1:c.7527T>C	XP_011541131.1:p.Tyr2509=
XM_011542830.1:c.7524T>C	XP_011541132.1:p.Tyr2508=
XM_011542831.1:c.7518T>C	XP_011541133.1:p.Tyr2506=
XM_011542832.1:c.5334T>C	XP_011541134.1:p.Tyr1778=
XM_011542833.1:c.5010T>C	XP_011541135.1:p.Tyr1670=
XM_006718839.3:c.4911T>C	XP_006718902.2:p.Tyr1637=
XM_011542829.2:c.7527T>C	XP_011541131.1:p.Tyr2509=
XM_011542830.2:c.7524T>C	XP_011541132.1:p.Tyr2508=
XM_011542831.2:c.7518T>C	XP_011541133.1:p.Tyr2506=
XM_011542833.2:c.5010T>C	XP_011541135.1:p.Tyr1670=
NM_001197104.2:c.7428T>C MANE Select	NP_001184033.1:p.Tyr2476=
NM_005933.4:c.7419T>C	NP_005924.2:p.Tyr2473=