Canonical Allele Identifier: CA2609913974
Gene: MAT1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80280397_80280401dup , CM000672.2:g.80280397_80280401dup GRCh38
NC_000010.10:g.82040153_82040157dup , CM000672.1:g.82040153_82040157dup GRCh37
NC_000010.9:g.82030133_82030137dup NCBI36
NG_008083.1:g.14280_14284dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.406-83_406-79dup MANE Select ENSP00000361287.3:n.406-83_406-79dup
ENST00000372213.7:c.406-83_406-79dup ENSP00000361287.3:n.406-83_406-79dup
ENST00000455001.1:c.217-83_217-79dup ENSP00000414961.1:n.217-83_217-79dup
NM_000429.2:c.406-83_406-79dup NP_000420.1:n.406-83_406-79dup
XM_005269842.3:c.406-83_406-79dup XP_005269899.1:n.406-83_406-79dup
XM_005269843.3:c.283-83_283-79dup XP_005269900.1:n.283-83_283-79dup
NM_000429.3:c.406-83_406-79dup MANE Select NP_000420.1:n.406-83_406-79dup