Canonical Allele Identifier: CA477091623

Gene: KMT2A

Linked Data

• gnomAD v4: 11-118491218-C-T
• MyVariant Identifiers: chr11:g.118361933C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118491218C>T , CM000673.2:g.118491218C>T	GRCh38
NC_000011.9:g.118361933C>T , CM000673.1:g.118361933C>T	GRCh37
NC_000011.8:g.117867143C>T	NCBI36
NG_027813.1:g.59729C>T , LRG_613:g.59729C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000531904.7:c.4818C>T	ENSP00000432391.3:p.Asp1606=
ENST00000710560.1:c.4818C>T	ENSP00000518343.1:p.Asp1606=
ENST00000685498.1:c.495C>T	ENSP00000509293.1:p.Asp165=
ENST00000691053.1:c.4719C>T	ENSP00000509168.1:p.Asp1573=
ENST00000389506.10:c.4719C>T	ENSP00000374157.5:p.Asp1573=
ENST00000534358.8:c.4719C>T MANE Select	ENSP00000436786.2:p.Asp1573=
ENST00000649699.1:c.4605C>T	ENSP00000496927.1:p.Asp1535=
ENST00000389506.9:c.4719C>T	ENSP00000374157.5:p.Asp1573=
ENST00000392873.3:c.855C>T	ENSP00000376612.3:p.Asp285=
ENST00000534358.5:c.4719C>T	ENSP00000436786.1:p.Asp1573=
NM_001197104.1:c.4719C>T , LRG_613t1:c.4719C>T	NP_001184033.1:p.Asp1573=
NM_005933.3:c.4719C>T	NP_005924.2:p.Asp1573=
XM_006718839.2:c.2202C>T	XP_006718902.2:p.Asp734=
XM_011542829.1:c.4818C>T	XP_011541131.1:p.Asp1606=
XM_011542830.1:c.4815C>T	XP_011541132.1:p.Asp1605=
XM_011542831.1:c.4818C>T	XP_011541133.1:p.Asp1606=
XM_011542832.1:c.2625C>T	XP_011541134.1:p.Asp875=
XM_011542833.1:c.2301C>T	XP_011541135.1:p.Asp767=
XM_006718839.3:c.2202C>T	XP_006718902.2:p.Asp734=
XM_011542829.2:c.4818C>T	XP_011541131.1:p.Asp1606=
XM_011542830.2:c.4815C>T	XP_011541132.1:p.Asp1605=
XM_011542831.2:c.4818C>T	XP_011541133.1:p.Asp1606=
XM_011542833.2:c.2301C>T	XP_011541135.1:p.Asp767=
NM_001197104.2:c.4719C>T MANE Select	NP_001184033.1:p.Asp1573=
NM_005933.4:c.4719C>T	NP_005924.2:p.Asp1573=