Canonical Allele Identifier: CA1922577984
Gene: MAT1A HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80280404C= , CM000672.2:g.80280404C= GRCh38
NC_000010.10:g.82040160C= , CM000672.1:g.82040160C= GRCh37
NC_000010.9:g.82030140C= NCBI36
NG_008083.1:g.14275G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.406-88G= MANE Select ENSP00000361287.3:n.406-88G=
ENST00000372213.7:c.406-88G= ENSP00000361287.3:n.406-88G=
ENST00000455001.1:c.217-88G= ENSP00000414961.1:n.217-88G=
NM_000429.2:c.406-88G= NP_000420.1:n.406-88G=
XM_005269842.3:c.406-88G= XP_005269899.1:n.406-88G=
XM_005269843.3:c.283-88G= XP_005269900.1:n.283-88G=
NM_000429.3:c.406-88G= MANE Select NP_000420.1:n.406-88G=
Search 100 bp 5'
Search 100 bp 3'