Canonical Allele Identifier: CA377362769

Gene: MAT1A

Linked Data

• dbSNP Id: rs2132705764
• MyVariant Identifiers: chr10:g.82040017A>G (hg19) ; chr10:g.80280261A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.80280261A>G , CM000672.2:g.80280261A>G	GRCh38
NC_000010.10:g.82040017A>G , CM000672.1:g.82040017A>G	GRCh37
NC_000010.9:g.82029997A>G	NCBI36
NG_008083.1:g.14418T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372213.8:c.461T>C MANE Select	ENSP00000361287.3:p.Ile154Thr
ENST00000372213.7:c.461T>C	ENSP00000361287.3:p.Ile154Thr
ENST00000455001.1:c.272T>C	ENSP00000414961.1:p.Ile91Thr
NM_000429.2:c.461T>C	NP_000420.1:p.Ile154Thr
XM_005269842.3:c.461T>C	XP_005269899.1:p.Ile154Thr
XM_005269843.3:c.338T>C	XP_005269900.1:p.Ile113Thr
NM_000429.3:c.461T>C MANE Select	NP_000420.1:p.Ile154Thr