Canonical Allele Identifier: CA377362868
Gene: MAT1A HGNC NCBI

Linked Data

dbSNP Id: rs369884238

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80280305G>C , CM000672.2:g.80280305G>C GRCh38
NC_000010.10:g.82040061G>C , CM000672.1:g.82040061G>C GRCh37
NC_000010.9:g.82030041G>C NCBI36
NG_008083.1:g.14374C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.417C>G MANE Select ENSP00000361287.3:p.Phe139Leu
ENST00000372213.7:c.417C>G ENSP00000361287.3:p.Phe139Leu
ENST00000455001.1:c.228C>G ENSP00000414961.1:p.Phe76Leu
NM_000429.2:c.417C>G NP_000420.1:p.Phe139Leu
XM_005269842.3:c.417C>G XP_005269899.1:p.Phe139Leu
XM_005269843.3:c.294C>G XP_005269900.1:p.Phe98Leu
NM_000429.3:c.417C>G MANE Select NP_000420.1:p.Phe139Leu