Canonical Allele Identifier: CA470468739

Gene: MAT1A

Linked Data

• MyVariant Identifiers: chr10:g.82040067C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.80280311C>T , CM000672.2:g.80280311C>T	GRCh38
NC_000010.10:g.82040067C>T , CM000672.1:g.82040067C>T	GRCh37
NC_000010.9:g.82030047C>T	NCBI36
NG_008083.1:g.14368G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372213.8:c.411G>A MANE Select	ENSP00000361287.3:p.Leu137=
ENST00000372213.7:c.411G>A	ENSP00000361287.3:p.Leu137=
ENST00000455001.1:c.222G>A	ENSP00000414961.1:p.Leu74=
NM_000429.2:c.411G>A	NP_000420.1:p.Leu137=
XM_005269842.3:c.411G>A	XP_005269899.1:p.Leu137=
XM_005269843.3:c.288G>A	XP_005269900.1:p.Leu96=
NM_000429.3:c.411G>A MANE Select	NP_000420.1:p.Leu137=