Canonical Allele Identifier: CA382806003
Gene: KMT2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118503444C>G , CM000673.2:g.118503444C>G GRCh38
NC_000011.9:g.118374159C>G , CM000673.1:g.118374159C>G GRCh37
NC_000011.8:g.117879369C>G NCBI36
NG_027813.1:g.71955C>G , LRG_613:g.71955C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000531904.7:c.7651C>G ENSP00000432391.3:p.Pro2551Ala
ENST00000710560.1:c.7642C>G ENSP00000518343.1:p.Pro2548Ala
ENST00000649878.2:c.1591C>G ENSP00000497891.2:p.Pro531Ala
ENST00000685397.1:c.1591C>G ENSP00000509586.1:p.Pro531Ala
ENST00000686370.1:c.1591C>G ENSP00000509179.1:p.Pro531Ala
ENST00000689424.1:c.1849C>G ENSP00000509852.1:p.Pro617Ala
ENST00000691053.1:c.7624C>G ENSP00000509168.1:p.Pro2542Ala
ENST00000389506.10:c.7543C>G ENSP00000374157.5:p.Pro2515Ala
ENST00000528278.2:n.6894C>G
ENST00000534358.8:c.7552C>G MANE Select ENSP00000436786.2:p.Pro2518Ala
ENST00000649699.1:c.7429C>G ENSP00000496927.1:p.Pro2477Ala
ENST00000389506.9:c.7543C>G ENSP00000374157.5:p.Pro2515Ala
ENST00000528278.1:n.1679C>G
ENST00000534358.5:c.7552C>G ENSP00000436786.1:p.Pro2518Ala
NM_001197104.1:c.7552C>G , LRG_613t1:c.7552C>G NP_001184033.1:p.Pro2518Ala
NM_005933.3:c.7543C>G NP_005924.2:p.Pro2515Ala
XM_006718839.2:c.5035C>G XP_006718902.2:p.Pro1679Ala
XM_011542829.1:c.7651C>G XP_011541131.1:p.Pro2551Ala
XM_011542830.1:c.7648C>G XP_011541132.1:p.Pro2550Ala
XM_011542831.1:c.7642C>G XP_011541133.1:p.Pro2548Ala
XM_011542832.1:c.5458C>G XP_011541134.1:p.Pro1820Ala
XM_011542833.1:c.5134C>G XP_011541135.1:p.Pro1712Ala
XM_006718839.3:c.5035C>G XP_006718902.2:p.Pro1679Ala
XM_011542829.2:c.7651C>G XP_011541131.1:p.Pro2551Ala
XM_011542830.2:c.7648C>G XP_011541132.1:p.Pro2550Ala
XM_011542831.2:c.7642C>G XP_011541133.1:p.Pro2548Ala
XM_011542833.2:c.5134C>G XP_011541135.1:p.Pro1712Ala
NM_001197104.2:c.7552C>G MANE Select NP_001184033.1:p.Pro2518Ala
NM_005933.4:c.7543C>G NP_005924.2:p.Pro2515Ala