Canonical Allele Identifier: CA1922574285
Gene: MAT1A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80276109T= , CM000672.2:g.80276109T= GRCh38
NC_000010.10:g.82035865T= , CM000672.1:g.82035865T= GRCh37
NC_000010.9:g.82025845T= NCBI36
NG_008083.1:g.18570A=

Transcript Alleles

HGVS Amino-acid change
ENST00000372213.8:c.768+267A= MANE Select ENSP00000361287.3:n.768+267A=
ENST00000372213.7:c.768+267A= ENSP00000361287.3:n.768+267A=
NM_000429.2:c.768+267A= NP_000420.1:n.768+267A=
XM_005269842.3:c.768+267A= XP_005269899.1:n.768+267A=
XM_005269843.3:c.645+267A= XP_005269900.1:n.645+267A=
NM_000429.3:c.768+267A= MANE Select NP_000420.1:n.768+267A=
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