Canonical Allele Identifier: CA1922573190
Gene: MAT1A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80274935G= , CM000672.2:g.80274935G= GRCh38
NC_000010.10:g.82034691G= , CM000672.1:g.82034691G= GRCh37
NC_000010.9:g.82024671G= NCBI36
NG_008083.1:g.19744C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.951+82C= MANE Select ENSP00000361287.3:n.951+82C=
ENST00000372213.7:c.951+82C= ENSP00000361287.3:n.951+82C=
ENST00000480845.1:n.183+82C=
ENST00000485270.5:n.463+82C=
NM_000429.2:c.951+82C= NP_000420.1:n.951+82C=
XM_005269842.3:c.951+82C= XP_005269899.1:n.951+82C=
XM_005269843.3:c.828+82C= XP_005269900.1:n.828+82C=
NM_000429.3:c.951+82C= MANE Select NP_000420.1:n.951+82C=
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