Canonical Allele Identifier: CA470467196
Gene: MAT1A HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.82033615G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80273859G>A , CM000672.2:g.80273859G>A GRCh38
NC_000010.10:g.82033615G>A , CM000672.1:g.82033615G>A GRCh37
NC_000010.9:g.82023595G>A NCBI36
NG_008083.1:g.20820C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000372213.8:c.1110C>T MANE Select ENSP00000361287.3:p.Ile370=
ENST00000372213.7:c.1110C>T ENSP00000361287.3:p.Ile370=
ENST00000480845.1:n.342C>T
ENST00000485270.5:n.622C>T
NM_000429.2:c.1110C>T NP_000420.1:p.Ile370=
XM_005269842.3:c.1110C>T XP_005269899.1:p.Ile370=
XM_005269843.3:c.987C>T XP_005269900.1:p.Ile329=
NM_000429.3:c.1110C>T MANE Select NP_000420.1:p.Ile370=