Canonical Allele Identifier: CA382805800

Gene: KMT2A

Linked Data

• MyVariant Identifiers: chr11:g.118374103G>C (hg19) ; chr11:g.118503388G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503388G>C , CM000673.2:g.118503388G>C	GRCh38
NC_000011.9:g.118374103G>C , CM000673.1:g.118374103G>C	GRCh37
NC_000011.8:g.117879313G>C	NCBI36
NG_027813.1:g.71899G>C , LRG_613:g.71899G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.7595G>C	ENSP00000432391.3:p.Gly2532Ala
ENST00000710560.1:c.7586G>C	ENSP00000518343.1:p.Gly2529Ala
ENST00000649878.2:c.1535G>C	ENSP00000497891.2:p.Gly512Ala
ENST00000685397.1:c.1535G>C	ENSP00000509586.1:p.Gly512Ala
ENST00000686370.1:c.1535G>C	ENSP00000509179.1:p.Gly512Ala
ENST00000689424.1:c.1793G>C	ENSP00000509852.1:p.Gly598Ala
ENST00000691053.1:c.7568G>C	ENSP00000509168.1:p.Gly2523Ala
ENST00000389506.10:c.7487G>C	ENSP00000374157.5:p.Gly2496Ala
ENST00000528278.2:n.6838G>C
ENST00000534358.8:c.7496G>C MANE Select	ENSP00000436786.2:p.Gly2499Ala
ENST00000649699.1:c.7373G>C	ENSP00000496927.1:p.Gly2458Ala
ENST00000389506.9:c.7487G>C	ENSP00000374157.5:p.Gly2496Ala
ENST00000528278.1:n.1623G>C
ENST00000534358.5:c.7496G>C	ENSP00000436786.1:p.Gly2499Ala
NM_001197104.1:c.7496G>C , LRG_613t1:c.7496G>C	NP_001184033.1:p.Gly2499Ala
NM_005933.3:c.7487G>C	NP_005924.2:p.Gly2496Ala
XM_006718839.2:c.4979G>C	XP_006718902.2:p.Gly1660Ala
XM_011542829.1:c.7595G>C	XP_011541131.1:p.Gly2532Ala
XM_011542830.1:c.7592G>C	XP_011541132.1:p.Gly2531Ala
XM_011542831.1:c.7586G>C	XP_011541133.1:p.Gly2529Ala
XM_011542832.1:c.5402G>C	XP_011541134.1:p.Gly1801Ala
XM_011542833.1:c.5078G>C	XP_011541135.1:p.Gly1693Ala
XM_006718839.3:c.4979G>C	XP_006718902.2:p.Gly1660Ala
XM_011542829.2:c.7595G>C	XP_011541131.1:p.Gly2532Ala
XM_011542830.2:c.7592G>C	XP_011541132.1:p.Gly2531Ala
XM_011542831.2:c.7586G>C	XP_011541133.1:p.Gly2529Ala
XM_011542833.2:c.5078G>C	XP_011541135.1:p.Gly1693Ala
NM_001197104.2:c.7496G>C MANE Select	NP_001184033.1:p.Gly2499Ala
NM_005933.4:c.7487G>C	NP_005924.2:p.Gly2496Ala