Canonical Allele Identifier: CA2536609469
Gene: MAT1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80280420_80280421insAT , CM000672.2:g.80280420_80280421insAT GRCh38
NC_000010.10:g.82040176_82040177insAT , CM000672.1:g.82040176_82040177insAT GRCh37
NC_000010.9:g.82030156_82030157insAT NCBI36
NG_008083.1:g.14258_14259insAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.406-105_406-104insAT MANE Select ENSP00000361287.3:n.406-105_406-104insAT
ENST00000372213.7:c.406-105_406-104insAT ENSP00000361287.3:n.406-105_406-104insAT
ENST00000455001.1:c.217-105_217-104insAT ENSP00000414961.1:n.217-105_217-104insAT
NM_000429.2:c.406-105_406-104insAT NP_000420.1:n.406-105_406-104insAT
XM_005269842.3:c.406-105_406-104insAT XP_005269899.1:n.406-105_406-104insAT
XM_005269843.3:c.283-105_283-104insAT XP_005269900.1:n.283-105_283-104insAT
NM_000429.3:c.406-105_406-104insAT MANE Select NP_000420.1:n.406-105_406-104insAT