Canonical Allele Identifier: CA377360180
Gene: MAT1A HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.82033614A>C (hg19) chr10:g.80273858A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80273858A>C , CM000672.2:g.80273858A>C GRCh38
NC_000010.10:g.82033614A>C , CM000672.1:g.82033614A>C GRCh37
NC_000010.9:g.82023594A>C NCBI36
NG_008083.1:g.20821T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.1111T>G MANE Select ENSP00000361287.3:p.Tyr371Asp
ENST00000372213.7:c.1111T>G ENSP00000361287.3:p.Tyr371Asp
ENST00000480845.1:n.343T>G
ENST00000485270.5:n.623T>G
NM_000429.2:c.1111T>G NP_000420.1:p.Tyr371Asp
XM_005269842.3:c.1111T>G XP_005269899.1:p.Tyr371Asp
XM_005269843.3:c.988T>G XP_005269900.1:p.Tyr330Asp
NM_000429.3:c.1111T>G MANE Select NP_000420.1:p.Tyr371Asp
Search 100 bp 5'
Search 100 bp 3'