Canonical Allele Identifier: CA1922578022
Gene: MAT1A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80280466T= , CM000672.2:g.80280466T= GRCh38
NC_000010.10:g.82040222T= , CM000672.1:g.82040222T= GRCh37
NC_000010.9:g.82030202T= NCBI36
NG_008083.1:g.14213A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.406-150A= MANE Select ENSP00000361287.3:n.406-150A=
ENST00000372213.7:c.406-150A= ENSP00000361287.3:n.406-150A=
ENST00000455001.1:c.217-150A= ENSP00000414961.1:n.217-150A=
NM_000429.2:c.406-150A= NP_000420.1:n.406-150A=
XM_005269842.3:c.406-150A= XP_005269899.1:n.406-150A=
XM_005269843.3:c.283-150A= XP_005269900.1:n.283-150A=
NM_000429.3:c.406-150A= MANE Select NP_000420.1:n.406-150A=
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