Canonical Allele Identifier: CA1922576728
Gene: MAT1A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80273431C= , CM000672.2:g.80273431C= GRCh38
NC_000010.10:g.82033187C= , CM000672.1:g.82033187C= GRCh37
NC_000010.9:g.82023167C= NCBI36
NG_008083.1:g.21248G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.*350G= MANE Select ENSP00000361287.3:n.*350G=
ENST00000372213.7:c.*350G= ENSP00000361287.3:n.*350G=
ENST00000480845.1:n.620+150G=
ENST00000485270.5:n.1050G=
NM_000429.2:c.*350G= NP_000420.1:n.*350G=
XM_005269842.3:c.*350G= XP_005269899.1:n.*350G=
XM_005269843.3:c.*350G= XP_005269900.1:n.*350G=
NM_000429.3:c.*350G= MANE Select NP_000420.1:n.*350G=
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