Canonical Allele Identifier: CA1922573176
Gene: MAT1A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80274919A= , CM000672.2:g.80274919A= GRCh38
NC_000010.10:g.82034675A= , CM000672.1:g.82034675A= GRCh37
NC_000010.9:g.82024655A= NCBI36
NG_008083.1:g.19760T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.951+98T= MANE Select ENSP00000361287.3:n.951+98T=
ENST00000372213.7:c.951+98T= ENSP00000361287.3:n.951+98T=
ENST00000480845.1:n.183+98T=
ENST00000485270.5:n.463+98T=
NM_000429.2:c.951+98T= NP_000420.1:n.951+98T=
XM_005269842.3:c.951+98T= XP_005269899.1:n.951+98T=
XM_005269843.3:c.828+98T= XP_005269900.1:n.828+98T=
NM_000429.3:c.951+98T= MANE Select NP_000420.1:n.951+98T=
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