Canonical Allele Identifier: CA2609913411
Gene: MAT1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80274998G>A , CM000672.2:g.80274998G>A GRCh38
NC_000010.10:g.82034754G>A , CM000672.1:g.82034754G>A GRCh37
NC_000010.9:g.82024734G>A NCBI36
NG_008083.1:g.19681C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.951+19C>T MANE Select ENSP00000361287.3:n.951+19C>T
ENST00000372213.7:c.951+19C>T ENSP00000361287.3:n.951+19C>T
ENST00000480845.1:n.183+19C>T
ENST00000485270.5:n.463+19C>T
NM_000429.2:c.951+19C>T NP_000420.1:n.951+19C>T
XM_005269842.3:c.951+19C>T XP_005269899.1:n.951+19C>T
XM_005269843.3:c.828+19C>T XP_005269900.1:n.828+19C>T
NM_000429.3:c.951+19C>T MANE Select NP_000420.1:n.951+19C>T