Canonical Allele Identifier: CA5576702
Gene: MAT1A HGNC NCBI

Linked Data

dbSNP Id: rs138556525

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80275192G>C , CM000672.2:g.80275192G>C GRCh38
NC_000010.10:g.82034948G>C , CM000672.1:g.82034948G>C GRCh37
NC_000010.9:g.82024928G>C NCBI36
NG_008083.1:g.19487C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.776C>G MANE Select ENSP00000361287.3:p.Ala259Gly
ENST00000372213.7:c.776C>G ENSP00000361287.3:p.Ala259Gly
ENST00000480845.1:n.8C>G
ENST00000485270.5:n.288C>G
NM_000429.2:c.776C>G NP_000420.1:p.Ala259Gly
XM_005269842.3:c.776C>G XP_005269899.1:p.Ala259Gly
XM_005269843.3:c.653C>G XP_005269900.1:p.Ala218Gly
NM_000429.3:c.776C>G MANE Select NP_000420.1:p.Ala259Gly