Canonical Allele Identifier: CA477093527

Gene: KMT2A

Linked Data

• MyVariant Identifiers: chr11:g.118373282T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118502567T>C , CM000673.2:g.118502567T>C	GRCh38
NC_000011.9:g.118373282T>C , CM000673.1:g.118373282T>C	GRCh37
NC_000011.8:g.117878492T>C	NCBI36
NG_027813.1:g.71078T>C , LRG_613:g.71078T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000531904.7:c.6774T>C	ENSP00000432391.3:p.Asn2258=
ENST00000710560.1:c.6765T>C	ENSP00000518343.1:p.Asn2255=
ENST00000649878.2:c.714T>C	ENSP00000497891.2:p.Asn238=
ENST00000685397.1:c.714T>C	ENSP00000509586.1:p.Asn238=
ENST00000686370.1:c.714T>C	ENSP00000509179.1:p.Asn238=
ENST00000689424.1:c.972T>C	ENSP00000509852.1:p.Asn324=
ENST00000691053.1:c.6747T>C	ENSP00000509168.1:p.Asn2249=
ENST00000389506.10:c.6666T>C	ENSP00000374157.5:p.Asn2222=
ENST00000528278.2:n.6017T>C
ENST00000534358.8:c.6675T>C MANE Select	ENSP00000436786.2:p.Asn2225=
ENST00000649699.1:c.6552T>C	ENSP00000496927.1:p.Asn2184=
ENST00000389506.9:c.6666T>C	ENSP00000374157.5:p.Asn2222=
ENST00000528278.1:n.802T>C
ENST00000534358.5:c.6675T>C	ENSP00000436786.1:p.Asn2225=
NM_001197104.1:c.6675T>C , LRG_613t1:c.6675T>C	NP_001184033.1:p.Asn2225=
NM_005933.3:c.6666T>C	NP_005924.2:p.Asn2222=
XM_006718839.2:c.4158T>C	XP_006718902.2:p.Asn1386=
XM_011542829.1:c.6774T>C	XP_011541131.1:p.Asn2258=
XM_011542830.1:c.6771T>C	XP_011541132.1:p.Asn2257=
XM_011542831.1:c.6765T>C	XP_011541133.1:p.Asn2255=
XM_011542832.1:c.4581T>C	XP_011541134.1:p.Asn1527=
XM_011542833.1:c.4257T>C	XP_011541135.1:p.Asn1419=
XM_006718839.3:c.4158T>C	XP_006718902.2:p.Asn1386=
XM_011542829.2:c.6774T>C	XP_011541131.1:p.Asn2258=
XM_011542830.2:c.6771T>C	XP_011541132.1:p.Asn2257=
XM_011542831.2:c.6765T>C	XP_011541133.1:p.Asn2255=
XM_011542833.2:c.4257T>C	XP_011541135.1:p.Asn1419=
NM_001197104.2:c.6675T>C MANE Select	NP_001184033.1:p.Asn2225=
NM_005933.4:c.6666T>C	NP_005924.2:p.Asn2222=