Canonical Allele Identifier: CA1922573834
Gene: MAT1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80275483_80275484delinsCT , CM000672.2:g.80275483_80275484delinsCT GRCh38
NC_000010.10:g.82035239_82035240delinsCT , CM000672.1:g.82035239_82035240delinsCT GRCh37
NC_000010.9:g.82025219_82025220delinsCT NCBI36
NG_008083.1:g.19195_19196delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.769-285_769-284delinsAG MANE Select ENSP00000361287.3:n.769-285_769-284delinsAG
ENST00000372213.7:c.769-285_769-284delinsAG ENSP00000361287.3:n.769-285_769-284delinsAG
NM_000429.2:c.769-285_769-284delinsAG NP_000420.1:n.769-285_769-284delinsAG
XM_005269842.3:c.769-285_769-284delinsAG XP_005269899.1:n.769-285_769-284delinsAG
XM_005269843.3:c.646-285_646-284delinsAG XP_005269900.1:n.646-285_646-284delinsAG
NM_000429.3:c.769-285_769-284delinsAG MANE Select NP_000420.1:n.769-285_769-284delinsAG