Canonical Allele Identifier: CA1922577857
Gene: MAT1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80280201G= , CM000672.2:g.80280201G= GRCh38
NC_000010.10:g.82039957G= , CM000672.1:g.82039957G= GRCh37
NC_000010.9:g.82029937G= NCBI36
NG_008083.1:g.14478C=

Transcript Alleles

HGVS Amino-acid change
ENST00000372213.8:c.521C= MANE Select ENSP00000361287.3:p.Pro174=
ENST00000372213.7:c.521C= ENSP00000361287.3:p.Pro174=
ENST00000455001.1:c.332C= ENSP00000414961.1:p.Pro111=
NM_000429.2:c.521C= NP_000420.1:p.Pro174=
XM_005269842.3:c.521C= XP_005269899.1:p.Pro174=
XM_005269843.3:c.398C= XP_005269900.1:p.Pro133=
NM_000429.3:c.521C= MANE Select NP_000420.1:p.Pro174=