Canonical Allele Identifier: CA382834504

Gene: KMT2A

Linked Data

• MyVariant Identifiers: chr11:g.118362017T>A (hg19) ; chr11:g.118491302T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118491302T>A , CM000673.2:g.118491302T>A	GRCh38
NC_000011.9:g.118362017T>A , CM000673.1:g.118362017T>A	GRCh37
NC_000011.8:g.117867227T>A	NCBI36
NG_027813.1:g.59813T>A , LRG_613:g.59813T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.4902T>A	ENSP00000432391.3:p.Asn1634Lys
ENST00000710560.1:c.4902T>A	ENSP00000518343.1:p.Asn1634Lys
ENST00000685498.1:c.579T>A	ENSP00000509293.1:p.Asn193Lys
ENST00000691053.1:c.4803T>A	ENSP00000509168.1:p.Asn1601Lys
ENST00000389506.10:c.4803T>A	ENSP00000374157.5:p.Asn1601Lys
ENST00000534358.8:c.4803T>A MANE Select	ENSP00000436786.2:p.Asn1601Lys
ENST00000649699.1:c.4689T>A	ENSP00000496927.1:p.Asn1563Lys
ENST00000389506.9:c.4803T>A	ENSP00000374157.5:p.Asn1601Lys
ENST00000392873.3:c.939T>A	ENSP00000376612.3:p.Asn313Lys
ENST00000534358.5:c.4803T>A	ENSP00000436786.1:p.Asn1601Lys
NM_001197104.1:c.4803T>A , LRG_613t1:c.4803T>A	NP_001184033.1:p.Asn1601Lys
NM_005933.3:c.4803T>A	NP_005924.2:p.Asn1601Lys
XM_006718839.2:c.2286T>A	XP_006718902.2:p.Asn762Lys
XM_011542829.1:c.4902T>A	XP_011541131.1:p.Asn1634Lys
XM_011542830.1:c.4899T>A	XP_011541132.1:p.Asn1633Lys
XM_011542831.1:c.4902T>A	XP_011541133.1:p.Asn1634Lys
XM_011542832.1:c.2709T>A	XP_011541134.1:p.Asn903Lys
XM_011542833.1:c.2385T>A	XP_011541135.1:p.Asn795Lys
XM_006718839.3:c.2286T>A	XP_006718902.2:p.Asn762Lys
XM_011542829.2:c.4902T>A	XP_011541131.1:p.Asn1634Lys
XM_011542830.2:c.4899T>A	XP_011541132.1:p.Asn1633Lys
XM_011542831.2:c.4902T>A	XP_011541133.1:p.Asn1634Lys
XM_011542833.2:c.2385T>A	XP_011541135.1:p.Asn795Lys
NM_001197104.2:c.4803T>A MANE Select	NP_001184033.1:p.Asn1601Lys
NM_005933.4:c.4803T>A	NP_005924.2:p.Asn1601Lys