Canonical Allele Identifier: CA2003527522

Gene: KMT2A

Linked Data

• dbSNP Id: rs1950529001

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503176_118503178del , CM000673.2:g.118503176_118503178del	GRCh38
NC_000011.9:g.118373891_118373893del , CM000673.1:g.118373891_118373893del	GRCh37
NC_000011.8:g.117879101_117879103del	NCBI36
NG_027813.1:g.71687_71689del , LRG_613:g.71687_71689del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.7383_7385del	ENSP00000432391.3:p.Arg2462del
ENST00000710560.1:c.7374_7376del	ENSP00000518343.1:p.Arg2459del
ENST00000649878.2:c.1323_1325del	ENSP00000497891.2:p.Arg442del
ENST00000685397.1:c.1323_1325del	ENSP00000509586.1:p.Arg442del
ENST00000686370.1:c.1323_1325del	ENSP00000509179.1:p.Arg442del
ENST00000689424.1:c.1581_1583del	ENSP00000509852.1:p.Arg528del
ENST00000691053.1:c.7356_7358del	ENSP00000509168.1:p.Arg2453del
ENST00000389506.10:c.7275_7277del	ENSP00000374157.5:p.Arg2426del
ENST00000528278.2:n.6626_6628del
ENST00000534358.8:c.7284_7286del MANE Select	ENSP00000436786.2:p.Arg2429del
ENST00000649699.1:c.7161_7163del	ENSP00000496927.1:p.Arg2388del
ENST00000389506.9:c.7275_7277del	ENSP00000374157.5:p.Arg2426del
ENST00000528278.1:n.1411_1413del
ENST00000534358.5:c.7284_7286del	ENSP00000436786.1:p.Arg2429del
NM_001197104.1:c.7284_7286del , LRG_613t1:c.7284_7286del	NP_001184033.1:p.Arg2429del
NM_005933.3:c.7275_7277del	NP_005924.2:p.Arg2426del
XM_006718839.2:c.4767_4769del	XP_006718902.2:p.Arg1590del
XM_011542829.1:c.7383_7385del	XP_011541131.1:p.Arg2462del
XM_011542830.1:c.7380_7382del	XP_011541132.1:p.Arg2461del
XM_011542831.1:c.7374_7376del	XP_011541133.1:p.Arg2459del
XM_011542832.1:c.5190_5192del	XP_011541134.1:p.Arg1731del
XM_011542833.1:c.4866_4868del	XP_011541135.1:p.Arg1623del
XM_006718839.3:c.4767_4769del	XP_006718902.2:p.Arg1590del
XM_011542829.2:c.7383_7385del	XP_011541131.1:p.Arg2462del
XM_011542830.2:c.7380_7382del	XP_011541132.1:p.Arg2461del
XM_011542831.2:c.7374_7376del	XP_011541133.1:p.Arg2459del
XM_011542833.2:c.4866_4868del	XP_011541135.1:p.Arg1623del
NM_001197104.2:c.7284_7286del MANE Select	NP_001184033.1:p.Arg2429del
NM_005933.4:c.7275_7277del	NP_005924.2:p.Arg2426del