Canonical Allele Identifier: CA377360514
Gene: MAT1A HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.82034403A>C (hg19) chr10:g.80274647A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80274647A>C , CM000672.2:g.80274647A>C GRCh38
NC_000010.10:g.82034403A>C , CM000672.1:g.82034403A>C GRCh37
NC_000010.9:g.82024383A>C NCBI36
NG_008083.1:g.20032T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000372213.8:c.958T>G MANE Select ENSP00000361287.3:p.Tyr320Asp
ENST00000372213.7:c.958T>G ENSP00000361287.3:p.Tyr320Asp
ENST00000480845.1:n.190T>G
ENST00000485270.5:n.470T>G
NM_000429.2:c.958T>G NP_000420.1:p.Tyr320Asp
XM_005269842.3:c.958T>G XP_005269899.1:p.Tyr320Asp
XM_005269843.3:c.835T>G XP_005269900.1:p.Tyr279Asp
NM_000429.3:c.958T>G MANE Select NP_000420.1:p.Tyr320Asp
Search 100 bp 5'
Search 100 bp 3'