Canonical Allele Identifier: CA1922577821
Gene: MAT1A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80274505C= , CM000672.2:g.80274505C= GRCh38
NC_000010.10:g.82034261C= , CM000672.1:g.82034261C= GRCh37
NC_000010.9:g.82024241C= NCBI36
NG_008083.1:g.20174G=

Transcript Alleles

HGVS Amino-acid change
ENST00000372213.8:c.1085+15G= MANE Select ENSP00000361287.3:n.1085+15G=
ENST00000372213.7:c.1085+15G= ENSP00000361287.3:n.1085+15G=
ENST00000480845.1:n.317+15G=
ENST00000485270.5:n.597+15G=
NM_000429.2:c.1085+15G= NP_000420.1:n.1085+15G=
XM_005269842.3:c.1085+15G= XP_005269899.1:n.1085+15G=
XM_005269843.3:c.962+15G= XP_005269900.1:n.962+15G=
NM_000429.3:c.1085+15G= MANE Select NP_000420.1:n.1085+15G=
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