Canonical Allele Identifier: CA1922576733
Gene: MAT1A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80273440G= , CM000672.2:g.80273440G= GRCh38
NC_000010.10:g.82033196G= , CM000672.1:g.82033196G= GRCh37
NC_000010.9:g.82023176G= NCBI36
NG_008083.1:g.21239C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.*341C= MANE Select ENSP00000361287.3:n.*341C=
ENST00000372213.7:c.*341C= ENSP00000361287.3:n.*341C=
ENST00000480845.1:n.620+141C=
ENST00000485270.5:n.1041C=
NM_000429.2:c.*341C= NP_000420.1:n.*341C=
XM_005269842.3:c.*341C= XP_005269899.1:n.*341C=
XM_005269843.3:c.*341C= XP_005269900.1:n.*341C=
NM_000429.3:c.*341C= MANE Select NP_000420.1:n.*341C=
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