Canonical Allele Identifier: CA477093528

Gene: KMT2A

Linked Data

• MyVariant Identifiers: chr11:g.118373288T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118502573T>A , CM000673.2:g.118502573T>A	GRCh38
NC_000011.9:g.118373288T>A , CM000673.1:g.118373288T>A	GRCh37
NC_000011.8:g.117878498T>A	NCBI36
NG_027813.1:g.71084T>A , LRG_613:g.71084T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.6780T>A	ENSP00000432391.3:p.Val2260=
ENST00000710560.1:c.6771T>A	ENSP00000518343.1:p.Val2257=
ENST00000649878.2:c.720T>A	ENSP00000497891.2:p.Val240=
ENST00000685397.1:c.720T>A	ENSP00000509586.1:p.Val240=
ENST00000686370.1:c.720T>A	ENSP00000509179.1:p.Val240=
ENST00000689424.1:c.978T>A	ENSP00000509852.1:p.Val326=
ENST00000691053.1:c.6753T>A	ENSP00000509168.1:p.Val2251=
ENST00000389506.10:c.6672T>A	ENSP00000374157.5:p.Val2224=
ENST00000528278.2:n.6023T>A
ENST00000534358.8:c.6681T>A MANE Select	ENSP00000436786.2:p.Val2227=
ENST00000649699.1:c.6558T>A	ENSP00000496927.1:p.Val2186=
ENST00000389506.9:c.6672T>A	ENSP00000374157.5:p.Val2224=
ENST00000528278.1:n.808T>A
ENST00000534358.5:c.6681T>A	ENSP00000436786.1:p.Val2227=
NM_001197104.1:c.6681T>A , LRG_613t1:c.6681T>A	NP_001184033.1:p.Val2227=
NM_005933.3:c.6672T>A	NP_005924.2:p.Val2224=
XM_006718839.2:c.4164T>A	XP_006718902.2:p.Val1388=
XM_011542829.1:c.6780T>A	XP_011541131.1:p.Val2260=
XM_011542830.1:c.6777T>A	XP_011541132.1:p.Val2259=
XM_011542831.1:c.6771T>A	XP_011541133.1:p.Val2257=
XM_011542832.1:c.4587T>A	XP_011541134.1:p.Val1529=
XM_011542833.1:c.4263T>A	XP_011541135.1:p.Val1421=
XM_006718839.3:c.4164T>A	XP_006718902.2:p.Val1388=
XM_011542829.2:c.6780T>A	XP_011541131.1:p.Val2260=
XM_011542830.2:c.6777T>A	XP_011541132.1:p.Val2259=
XM_011542831.2:c.6771T>A	XP_011541133.1:p.Val2257=
XM_011542833.2:c.4263T>A	XP_011541135.1:p.Val1421=
NM_001197104.2:c.6681T>A MANE Select	NP_001184033.1:p.Val2227=
NM_005933.4:c.6672T>A	NP_005924.2:p.Val2224=