Canonical Allele Identifier: CA477359465

Gene: KMT2A

Linked Data

• MyVariant Identifiers: chr11:g.118374101A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503386A>C , CM000673.2:g.118503386A>C	GRCh38
NC_000011.9:g.118374101A>C , CM000673.1:g.118374101A>C	GRCh37
NC_000011.8:g.117879311A>C	NCBI36
NG_027813.1:g.71897A>C , LRG_613:g.71897A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.7593A>C	ENSP00000432391.3:p.Pro2531=
ENST00000710560.1:c.7584A>C	ENSP00000518343.1:p.Pro2528=
ENST00000649878.2:c.1533A>C	ENSP00000497891.2:p.Pro511=
ENST00000685397.1:c.1533A>C	ENSP00000509586.1:p.Pro511=
ENST00000686370.1:c.1533A>C	ENSP00000509179.1:p.Pro511=
ENST00000689424.1:c.1791A>C	ENSP00000509852.1:p.Pro597=
ENST00000691053.1:c.7566A>C	ENSP00000509168.1:p.Pro2522=
ENST00000389506.10:c.7485A>C	ENSP00000374157.5:p.Pro2495=
ENST00000528278.2:n.6836A>C
ENST00000534358.8:c.7494A>C MANE Select	ENSP00000436786.2:p.Pro2498=
ENST00000649699.1:c.7371A>C	ENSP00000496927.1:p.Pro2457=
ENST00000389506.9:c.7485A>C	ENSP00000374157.5:p.Pro2495=
ENST00000528278.1:n.1621A>C
ENST00000534358.5:c.7494A>C	ENSP00000436786.1:p.Pro2498=
NM_001197104.1:c.7494A>C , LRG_613t1:c.7494A>C	NP_001184033.1:p.Pro2498=
NM_005933.3:c.7485A>C	NP_005924.2:p.Pro2495=
XM_006718839.2:c.4977A>C	XP_006718902.2:p.Pro1659=
XM_011542829.1:c.7593A>C	XP_011541131.1:p.Pro2531=
XM_011542830.1:c.7590A>C	XP_011541132.1:p.Pro2530=
XM_011542831.1:c.7584A>C	XP_011541133.1:p.Pro2528=
XM_011542832.1:c.5400A>C	XP_011541134.1:p.Pro1800=
XM_011542833.1:c.5076A>C	XP_011541135.1:p.Pro1692=
XM_006718839.3:c.4977A>C	XP_006718902.2:p.Pro1659=
XM_011542829.2:c.7593A>C	XP_011541131.1:p.Pro2531=
XM_011542830.2:c.7590A>C	XP_011541132.1:p.Pro2530=
XM_011542831.2:c.7584A>C	XP_011541133.1:p.Pro2528=
XM_011542833.2:c.5076A>C	XP_011541135.1:p.Pro1692=
NM_001197104.2:c.7494A>C MANE Select	NP_001184033.1:p.Pro2498=
NM_005933.4:c.7485A>C	NP_005924.2:p.Pro2495=