Canonical Allele Identifier: CA470467368

Gene: MAT1A

Linked Data

• MyVariant Identifiers: chr10:g.82034878G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.80275122G>A , CM000672.2:g.80275122G>A	GRCh38
NC_000010.10:g.82034878G>A , CM000672.1:g.82034878G>A	GRCh37
NC_000010.9:g.82024858G>A	NCBI36
NG_008083.1:g.19557C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372213.8:c.846C>T MANE Select	ENSP00000361287.3:p.Phe282=
ENST00000372213.7:c.846C>T	ENSP00000361287.3:p.Phe282=
ENST00000480845.1:n.78C>T
ENST00000485270.5:n.358C>T
NM_000429.2:c.846C>T	NP_000420.1:p.Phe282=
XM_005269842.3:c.846C>T	XP_005269899.1:p.Phe282=
XM_005269843.3:c.723C>T	XP_005269900.1:p.Phe241=
NM_000429.3:c.846C>T MANE Select	NP_000420.1:p.Phe282=