Canonical Allele Identifier: CA1922576819
Gene: MAT1A HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80273502T= , CM000672.2:g.80273502T= GRCh38
NC_000010.10:g.82033258T= , CM000672.1:g.82033258T= GRCh37
NC_000010.9:g.82023238T= NCBI36
NG_008083.1:g.21177A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.*279A= MANE Select ENSP00000361287.3:n.*279A=
ENST00000372213.7:c.*279A= ENSP00000361287.3:n.*279A=
ENST00000480845.1:n.620+79A=
ENST00000485270.5:n.979A=
NM_000429.2:c.*279A= NP_000420.1:n.*279A=
XM_005269842.3:c.*279A= XP_005269899.1:n.*279A=
XM_005269843.3:c.*279A= XP_005269900.1:n.*279A=
NM_000429.3:c.*279A= MANE Select NP_000420.1:n.*279A=
Search 100 bp 5'
Search 100 bp 3'