Canonical Allele Identifier: CA470468044
Gene: MAT1A HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.82039944A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80280188A>T , CM000672.2:g.80280188A>T GRCh38
NC_000010.10:g.82039944A>T , CM000672.1:g.82039944A>T GRCh37
NC_000010.9:g.82029924A>T NCBI36
NG_008083.1:g.14491T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.534T>A MANE Select ENSP00000361287.3:p.Pro178=
ENST00000372213.7:c.534T>A ENSP00000361287.3:p.Pro178=
ENST00000455001.1:c.345T>A ENSP00000414961.1:p.Pro115=
NM_000429.2:c.534T>A NP_000420.1:p.Pro178=
XM_005269842.3:c.534T>A XP_005269899.1:p.Pro178=
XM_005269843.3:c.411T>A XP_005269900.1:p.Pro137=
NM_000429.3:c.534T>A MANE Select NP_000420.1:p.Pro178=