Canonical Allele Identifier: CA1922578032
Gene: MAT1A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80280487G= , CM000672.2:g.80280487G= GRCh38
NC_000010.10:g.82040243G= , CM000672.1:g.82040243G= GRCh37
NC_000010.9:g.82030223G= NCBI36
NG_008083.1:g.14192C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.406-171C= MANE Select ENSP00000361287.3:n.406-171C=
ENST00000372213.7:c.406-171C= ENSP00000361287.3:n.406-171C=
ENST00000455001.1:c.217-171C= ENSP00000414961.1:n.217-171C=
NM_000429.2:c.406-171C= NP_000420.1:n.406-171C=
XM_005269842.3:c.406-171C= XP_005269899.1:n.406-171C=
XM_005269843.3:c.283-171C= XP_005269900.1:n.283-171C=
NM_000429.3:c.406-171C= MANE Select NP_000420.1:n.406-171C=
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