Canonical Allele Identifier: CA2360754991
Gene: SNTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33443533G= , CM000682.2:g.33443533G= GRCh38
NC_000020.10:g.32031339G= , CM000682.1:g.32031339G= GRCh37
NC_000020.9:g.31495000G= NCBI36
NG_011622.1:g.5360C= , LRG_332:g.5360C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.3:c.88C= MANE Select ENSP00000217381.2:p.Arg30=
ENST00000217381.2:c.88C= ENSP00000217381.2:p.Arg30=
NM_003098.2:c.88C= , LRG_332t1:c.88C= NP_003089.1:p.Arg30=
XM_005260517.1:c.88C= XP_005260574.1:p.Arg30=
XM_011529007.1:c.88C= XP_011527309.1:p.Arg30=
XM_011529008.1:c.88C= XP_011527310.1:p.Arg30=
XR_936612.1:n.321C=
NM_003098.3:c.88C= MANE Select NP_003089.1:p.Arg30=