Canonical Allele Identifier: CA477093500

Gene: KMT2A

Linked Data

• MyVariant Identifiers: chr11:g.118373240G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118502525G>C , CM000673.2:g.118502525G>C	GRCh38
NC_000011.9:g.118373240G>C , CM000673.1:g.118373240G>C	GRCh37
NC_000011.8:g.117878450G>C	NCBI36
NG_027813.1:g.71036G>C , LRG_613:g.71036G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.6732G>C	ENSP00000432391.3:p.Arg2244=
ENST00000710560.1:c.6723G>C	ENSP00000518343.1:p.Arg2241=
ENST00000649878.2:c.672G>C	ENSP00000497891.2:p.Arg224=
ENST00000685397.1:c.672G>C	ENSP00000509586.1:p.Arg224=
ENST00000686370.1:c.672G>C	ENSP00000509179.1:p.Arg224=
ENST00000689424.1:c.930G>C	ENSP00000509852.1:p.Arg310=
ENST00000691053.1:c.6705G>C	ENSP00000509168.1:p.Arg2235=
ENST00000389506.10:c.6624G>C	ENSP00000374157.5:p.Arg2208=
ENST00000528278.2:n.5975G>C
ENST00000534358.8:c.6633G>C MANE Select	ENSP00000436786.2:p.Arg2211=
ENST00000649699.1:c.6510G>C	ENSP00000496927.1:p.Arg2170=
ENST00000389506.9:c.6624G>C	ENSP00000374157.5:p.Arg2208=
ENST00000528278.1:n.760G>C
ENST00000534358.5:c.6633G>C	ENSP00000436786.1:p.Arg2211=
NM_001197104.1:c.6633G>C , LRG_613t1:c.6633G>C	NP_001184033.1:p.Arg2211=
NM_005933.3:c.6624G>C	NP_005924.2:p.Arg2208=
XM_006718839.2:c.4116G>C	XP_006718902.2:p.Arg1372=
XM_011542829.1:c.6732G>C	XP_011541131.1:p.Arg2244=
XM_011542830.1:c.6729G>C	XP_011541132.1:p.Arg2243=
XM_011542831.1:c.6723G>C	XP_011541133.1:p.Arg2241=
XM_011542832.1:c.4539G>C	XP_011541134.1:p.Arg1513=
XM_011542833.1:c.4215G>C	XP_011541135.1:p.Arg1405=
XM_006718839.3:c.4116G>C	XP_006718902.2:p.Arg1372=
XM_011542829.2:c.6732G>C	XP_011541131.1:p.Arg2244=
XM_011542830.2:c.6729G>C	XP_011541132.1:p.Arg2243=
XM_011542831.2:c.6723G>C	XP_011541133.1:p.Arg2241=
XM_011542833.2:c.4215G>C	XP_011541135.1:p.Arg1405=
NM_001197104.2:c.6633G>C MANE Select	NP_001184033.1:p.Arg2211=
NM_005933.4:c.6624G>C	NP_005924.2:p.Arg2208=