Canonical Allele Identifier: CA377360439
Gene: MAT1A HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.82034366A>C (hg19) chr10:g.80274610A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80274610A>C , CM000672.2:g.80274610A>C GRCh38
NC_000010.10:g.82034366A>C , CM000672.1:g.82034366A>C GRCh37
NC_000010.9:g.82024346A>C NCBI36
NG_008083.1:g.20069T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000372213.8:c.995T>G MANE Select ENSP00000361287.3:p.Ile332Ser
ENST00000372213.7:c.995T>G ENSP00000361287.3:p.Ile332Ser
ENST00000480845.1:n.227T>G
ENST00000485270.5:n.507T>G
NM_000429.2:c.995T>G NP_000420.1:p.Ile332Ser
XM_005269842.3:c.995T>G XP_005269899.1:p.Ile332Ser
XM_005269843.3:c.872T>G XP_005269900.1:p.Ile291Ser
NM_000429.3:c.995T>G MANE Select NP_000420.1:p.Ile332Ser
Search 100 bp 5'
Search 100 bp 3'