Canonical Allele Identifier: CA477091666

Gene: KMT2A

Linked Data

• gnomAD v4: 11-118491305-T-C
• MyVariant Identifiers: chr11:g.118362020T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118491305T>C , CM000673.2:g.118491305T>C	GRCh38
NC_000011.9:g.118362020T>C , CM000673.1:g.118362020T>C	GRCh37
NC_000011.8:g.117867230T>C	NCBI36
NG_027813.1:g.59816T>C , LRG_613:g.59816T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.4905T>C	ENSP00000432391.3:p.Leu1635=
ENST00000710560.1:c.4905T>C	ENSP00000518343.1:p.Leu1635=
ENST00000685498.1:c.582T>C	ENSP00000509293.1:p.Leu194=
ENST00000691053.1:c.4806T>C	ENSP00000509168.1:p.Leu1602=
ENST00000389506.10:c.4806T>C	ENSP00000374157.5:p.Leu1602=
ENST00000534358.8:c.4806T>C MANE Select	ENSP00000436786.2:p.Leu1602=
ENST00000649699.1:c.4692T>C	ENSP00000496927.1:p.Leu1564=
ENST00000389506.9:c.4806T>C	ENSP00000374157.5:p.Leu1602=
ENST00000392873.3:c.942T>C	ENSP00000376612.3:p.Leu314=
ENST00000534358.5:c.4806T>C	ENSP00000436786.1:p.Leu1602=
NM_001197104.1:c.4806T>C , LRG_613t1:c.4806T>C	NP_001184033.1:p.Leu1602=
NM_005933.3:c.4806T>C	NP_005924.2:p.Leu1602=
XM_006718839.2:c.2289T>C	XP_006718902.2:p.Leu763=
XM_011542829.1:c.4905T>C	XP_011541131.1:p.Leu1635=
XM_011542830.1:c.4902T>C	XP_011541132.1:p.Leu1634=
XM_011542831.1:c.4905T>C	XP_011541133.1:p.Leu1635=
XM_011542832.1:c.2712T>C	XP_011541134.1:p.Leu904=
XM_011542833.1:c.2388T>C	XP_011541135.1:p.Leu796=
XM_006718839.3:c.2289T>C	XP_006718902.2:p.Leu763=
XM_011542829.2:c.4905T>C	XP_011541131.1:p.Leu1635=
XM_011542830.2:c.4902T>C	XP_011541132.1:p.Leu1634=
XM_011542831.2:c.4905T>C	XP_011541133.1:p.Leu1635=
XM_011542833.2:c.2388T>C	XP_011541135.1:p.Leu796=
NM_001197104.2:c.4806T>C MANE Select	NP_001184033.1:p.Leu1602=
NM_005933.4:c.4806T>C	NP_005924.2:p.Leu1602=