Canonical Allele Identifier: CA377360046
Gene: MAT1A HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.82033557G>A (hg19) chr10:g.80273801G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80273801G>A , CM000672.2:g.80273801G>A GRCh38
NC_000010.10:g.82033557G>A , CM000672.1:g.82033557G>A GRCh37
NC_000010.9:g.82023537G>A NCBI36
NG_008083.1:g.20878C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.1168C>T MANE Select ENSP00000361287.3:p.Pro390Ser
ENST00000372213.7:c.1168C>T ENSP00000361287.3:p.Pro390Ser
ENST00000480845.1:n.400C>T
ENST00000485270.5:n.680C>T
NM_000429.2:c.1168C>T NP_000420.1:p.Pro390Ser
XM_005269842.3:c.1168C>T XP_005269899.1:p.Pro390Ser
XM_005269843.3:c.1045C>T XP_005269900.1:p.Pro349Ser
NM_000429.3:c.1168C>T MANE Select NP_000420.1:p.Pro390Ser
Search 100 bp 5'
Search 100 bp 3'