Canonical Allele Identifier: CA382802638

Gene: KMT2A

Linked Data

• MyVariant Identifiers: chr11:g.118373281A>C (hg19) ; chr11:g.118502566A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118502566A>C , CM000673.2:g.118502566A>C	GRCh38
NC_000011.9:g.118373281A>C , CM000673.1:g.118373281A>C	GRCh37
NC_000011.8:g.117878491A>C	NCBI36
NG_027813.1:g.71077A>C , LRG_613:g.71077A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000531904.7:c.6773A>C	ENSP00000432391.3:p.Asn2258Thr
ENST00000710560.1:c.6764A>C	ENSP00000518343.1:p.Asn2255Thr
ENST00000649878.2:c.713A>C	ENSP00000497891.2:p.Asn238Thr
ENST00000685397.1:c.713A>C	ENSP00000509586.1:p.Asn238Thr
ENST00000686370.1:c.713A>C	ENSP00000509179.1:p.Asn238Thr
ENST00000689424.1:c.971A>C	ENSP00000509852.1:p.Asn324Thr
ENST00000691053.1:c.6746A>C	ENSP00000509168.1:p.Asn2249Thr
ENST00000389506.10:c.6665A>C	ENSP00000374157.5:p.Asn2222Thr
ENST00000528278.2:n.6016A>C
ENST00000534358.8:c.6674A>C MANE Select	ENSP00000436786.2:p.Asn2225Thr
ENST00000649699.1:c.6551A>C	ENSP00000496927.1:p.Asn2184Thr
ENST00000389506.9:c.6665A>C	ENSP00000374157.5:p.Asn2222Thr
ENST00000528278.1:n.801A>C
ENST00000534358.5:c.6674A>C	ENSP00000436786.1:p.Asn2225Thr
NM_001197104.1:c.6674A>C , LRG_613t1:c.6674A>C	NP_001184033.1:p.Asn2225Thr
NM_005933.3:c.6665A>C	NP_005924.2:p.Asn2222Thr
XM_006718839.2:c.4157A>C	XP_006718902.2:p.Asn1386Thr
XM_011542829.1:c.6773A>C	XP_011541131.1:p.Asn2258Thr
XM_011542830.1:c.6770A>C	XP_011541132.1:p.Asn2257Thr
XM_011542831.1:c.6764A>C	XP_011541133.1:p.Asn2255Thr
XM_011542832.1:c.4580A>C	XP_011541134.1:p.Asn1527Thr
XM_011542833.1:c.4256A>C	XP_011541135.1:p.Asn1419Thr
XM_006718839.3:c.4157A>C	XP_006718902.2:p.Asn1386Thr
XM_011542829.2:c.6773A>C	XP_011541131.1:p.Asn2258Thr
XM_011542830.2:c.6770A>C	XP_011541132.1:p.Asn2257Thr
XM_011542831.2:c.6764A>C	XP_011541133.1:p.Asn2255Thr
XM_011542833.2:c.4256A>C	XP_011541135.1:p.Asn1419Thr
NM_001197104.2:c.6674A>C MANE Select	NP_001184033.1:p.Asn2225Thr
NM_005933.4:c.6665A>C	NP_005924.2:p.Asn2222Thr