Canonical Allele Identifier: CA6303914

Gene: KMT2A

Linked Data

• dbSNP Id: rs112836014
• ExAC: 11:118360879 A / T
• gnomAD v2: 11-118360879-A-T
• gnomAD v3: 11-118490164-A-T
• gnomAD v4: 11-118490164-A-T
• MyVariant Identifiers: chr11:g.118360879A>T (hg19) ; chr11:g.118490164A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118490164A>T , CM000673.2:g.118490164A>T	GRCh38
NC_000011.9:g.118360879A>T , CM000673.1:g.118360879A>T	GRCh37
NC_000011.8:g.117866089A>T	NCBI36
NG_027813.1:g.58675A>T , LRG_613:g.58675A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000531904.7:c.4710A>T	ENSP00000432391.3:p.Gly1570=
ENST00000710560.1:c.4710A>T	ENSP00000518343.1:p.Gly1570=
ENST00000685498.1:c.387A>T	ENSP00000509293.1:p.Gly129=
ENST00000691053.1:c.4611A>T	ENSP00000509168.1:p.Gly1537=
ENST00000389506.10:c.4611A>T	ENSP00000374157.5:p.Gly1537=
ENST00000534358.8:c.4611A>T MANE Select	ENSP00000436786.2:p.Gly1537=
ENST00000649699.1:c.4497A>T	ENSP00000496927.1:p.Gly1499=
ENST00000389506.9:c.4611A>T	ENSP00000374157.5:p.Gly1537=
ENST00000392873.3:c.747A>T	ENSP00000376612.3:p.Gly249=
ENST00000534358.5:c.4611A>T	ENSP00000436786.1:p.Gly1537=
NM_001197104.1:c.4611A>T , LRG_613t1:c.4611A>T	NP_001184033.1:p.Gly1537=
NM_005933.3:c.4611A>T	NP_005924.2:p.Gly1537=
XM_006718839.2:c.2094A>T	XP_006718902.2:p.Gly698=
XM_011542829.1:c.4710A>T	XP_011541131.1:p.Gly1570=
XM_011542830.1:c.4707A>T	XP_011541132.1:p.Gly1569=
XM_011542831.1:c.4710A>T	XP_011541133.1:p.Gly1570=
XM_011542832.1:c.2517A>T	XP_011541134.1:p.Gly839=
XM_011542833.1:c.2193A>T	XP_011541135.1:p.Gly731=
XM_006718839.3:c.2094A>T	XP_006718902.2:p.Gly698=
XM_011542829.2:c.4710A>T	XP_011541131.1:p.Gly1570=
XM_011542830.2:c.4707A>T	XP_011541132.1:p.Gly1569=
XM_011542831.2:c.4710A>T	XP_011541133.1:p.Gly1570=
XM_011542833.2:c.2193A>T	XP_011541135.1:p.Gly731=
NM_001197104.2:c.4611A>T MANE Select	NP_001184033.1:p.Gly1537=
NM_005933.4:c.4611A>T	NP_005924.2:p.Gly1537=