Canonical Allele Identifier: CA1922573733
Gene: MAT1A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80275351T= , CM000672.2:g.80275351T= GRCh38
NC_000010.10:g.82035107T= , CM000672.1:g.82035107T= GRCh37
NC_000010.9:g.82025087T= NCBI36
NG_008083.1:g.19328A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.769-152A= MANE Select ENSP00000361287.3:n.769-152A=
ENST00000372213.7:c.769-152A= ENSP00000361287.3:n.769-152A=
ENST00000485270.5:n.129A=
NM_000429.2:c.769-152A= NP_000420.1:n.769-152A=
XM_005269842.3:c.769-152A= XP_005269899.1:n.769-152A=
XM_005269843.3:c.646-152A= XP_005269900.1:n.646-152A=
NM_000429.3:c.769-152A= MANE Select NP_000420.1:n.769-152A=
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