Canonical Allele Identifier: CA382805614
Gene: KMT2A HGNC NCBI

Linked Data

dbSNP Id: rs1950531728

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118503340A>C , CM000673.2:g.118503340A>C GRCh38
NC_000011.9:g.118374055A>C , CM000673.1:g.118374055A>C GRCh37
NC_000011.8:g.117879265A>C NCBI36
NG_027813.1:g.71851A>C , LRG_613:g.71851A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000531904.7:c.7547A>C ENSP00000432391.3:p.Asn2516Thr
ENST00000710560.1:c.7538A>C ENSP00000518343.1:p.Asn2513Thr
ENST00000649878.2:c.1487A>C ENSP00000497891.2:p.Asn496Thr
ENST00000685397.1:c.1487A>C ENSP00000509586.1:p.Asn496Thr
ENST00000686370.1:c.1487A>C ENSP00000509179.1:p.Asn496Thr
ENST00000689424.1:c.1745A>C ENSP00000509852.1:p.Asn582Thr
ENST00000691053.1:c.7520A>C ENSP00000509168.1:p.Asn2507Thr
ENST00000389506.10:c.7439A>C ENSP00000374157.5:p.Asn2480Thr
ENST00000528278.2:n.6790A>C
ENST00000534358.8:c.7448A>C MANE Select ENSP00000436786.2:p.Asn2483Thr
ENST00000649699.1:c.7325A>C ENSP00000496927.1:p.Asn2442Thr
ENST00000389506.9:c.7439A>C ENSP00000374157.5:p.Asn2480Thr
ENST00000528278.1:n.1575A>C
ENST00000534358.5:c.7448A>C ENSP00000436786.1:p.Asn2483Thr
NM_001197104.1:c.7448A>C , LRG_613t1:c.7448A>C NP_001184033.1:p.Asn2483Thr
NM_005933.3:c.7439A>C NP_005924.2:p.Asn2480Thr
XM_006718839.2:c.4931A>C XP_006718902.2:p.Asn1644Thr
XM_011542829.1:c.7547A>C XP_011541131.1:p.Asn2516Thr
XM_011542830.1:c.7544A>C XP_011541132.1:p.Asn2515Thr
XM_011542831.1:c.7538A>C XP_011541133.1:p.Asn2513Thr
XM_011542832.1:c.5354A>C XP_011541134.1:p.Asn1785Thr
XM_011542833.1:c.5030A>C XP_011541135.1:p.Asn1677Thr
XM_006718839.3:c.4931A>C XP_006718902.2:p.Asn1644Thr
XM_011542829.2:c.7547A>C XP_011541131.1:p.Asn2516Thr
XM_011542830.2:c.7544A>C XP_011541132.1:p.Asn2515Thr
XM_011542831.2:c.7538A>C XP_011541133.1:p.Asn2513Thr
XM_011542833.2:c.5030A>C XP_011541135.1:p.Asn1677Thr
NM_001197104.2:c.7448A>C MANE Select NP_001184033.1:p.Asn2483Thr
NM_005933.4:c.7439A>C NP_005924.2:p.Asn2480Thr