Canonical Allele Identifier: CA1922573618
Gene: MAT1A HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80275209G= , CM000672.2:g.80275209G= GRCh38
NC_000010.10:g.82034965G= , CM000672.1:g.82034965G= GRCh37
NC_000010.9:g.82024945G= NCBI36
NG_008083.1:g.19470C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.769-10C= MANE Select ENSP00000361287.3:n.769-10C=
ENST00000372213.7:c.769-10C= ENSP00000361287.3:n.769-10C=
ENST00000485270.5:n.271C=
NM_000429.2:c.769-10C= NP_000420.1:n.769-10C=
XM_005269842.3:c.769-10C= XP_005269899.1:n.769-10C=
XM_005269843.3:c.646-10C= XP_005269900.1:n.646-10C=
NM_000429.3:c.769-10C= MANE Select NP_000420.1:n.769-10C=
Search 100 bp 5'
Search 100 bp 3'