Canonical Allele Identifier: CA377361577

Gene: MAT1A

Linked Data

• COSMIC: COSM920791
• MyVariant Identifiers: chr10:g.82036143C>A (hg19) ; chr10:g.80276387C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.80276387C>A , CM000672.2:g.80276387C>A	GRCh38
NC_000010.10:g.82036143C>A , CM000672.1:g.82036143C>A	GRCh37
NC_000010.9:g.82026123C>A	NCBI36
NG_008083.1:g.18292G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000372213.8:c.757G>T MANE Select	ENSP00000361287.3:p.Gly253Ter
ENST00000372213.7:c.757G>T	ENSP00000361287.3:p.Gly253Ter
NM_000429.2:c.757G>T	NP_000420.1:p.Gly253Ter
XM_005269842.3:c.757G>T	XP_005269899.1:p.Gly253Ter
XM_005269843.3:c.634G>T	XP_005269900.1:p.Gly212Ter
NM_000429.3:c.757G>T MANE Select	NP_000420.1:p.Gly253Ter