Canonical Allele Identifier: CA1922573771
Gene: MAT1A HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80275394A= , CM000672.2:g.80275394A= GRCh38
NC_000010.10:g.82035150A= , CM000672.1:g.82035150A= GRCh37
NC_000010.9:g.82025130A= NCBI36
NG_008083.1:g.19285T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.769-195T= MANE Select ENSP00000361287.3:n.769-195T=
ENST00000372213.7:c.769-195T= ENSP00000361287.3:n.769-195T=
ENST00000485270.5:n.86T=
NM_000429.2:c.769-195T= NP_000420.1:n.769-195T=
XM_005269842.3:c.769-195T= XP_005269899.1:n.769-195T=
XM_005269843.3:c.646-195T= XP_005269900.1:n.646-195T=
NM_000429.3:c.769-195T= MANE Select NP_000420.1:n.769-195T=
Search 100 bp 5'
Search 100 bp 3'