Canonical Allele Identifier: CA377360252
Gene: MAT1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80274518A>T , CM000672.2:g.80274518A>T GRCh38
NC_000010.10:g.82034274A>T , CM000672.1:g.82034274A>T GRCh37
NC_000010.9:g.82024254A>T NCBI36
NG_008083.1:g.20161T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000372213.8:c.1085+2T>A MANE Select ENSP00000361287.3:n.1085+2T>A
ENST00000372213.7:c.1085+2T>A ENSP00000361287.3:n.1085+2T>A
ENST00000480845.1:n.317+2T>A
ENST00000485270.5:n.597+2T>A
NM_000429.2:c.1085+2T>A NP_000420.1:n.1085+2T>A
XM_005269842.3:c.1085+2T>A XP_005269899.1:n.1085+2T>A
XM_005269843.3:c.962+2T>A XP_005269900.1:n.962+2T>A
NM_000429.3:c.1085+2T>A MANE Select NP_000420.1:n.1085+2T>A