Canonical Allele Identifier: CA2360740076
Gene: SNTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33408535T= , CM000682.2:g.33408535T= GRCh38
NC_000020.10:g.31996341T= , CM000682.1:g.31996341T= GRCh37
NC_000020.9:g.31460002T= NCBI36
NG_011622.1:g.40358A= , LRG_332:g.40358A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.3:c.1490A= MANE Select ENSP00000217381.2:p.Lys497=
ENST00000217381.2:c.1490A= ENSP00000217381.2:p.Lys497=
NM_003098.2:c.1490A= , LRG_332t1:c.1490A= NP_003089.1:p.Lys497=
XM_005260517.1:c.1487A= XP_005260574.1:p.Lys496=
XM_011529007.1:c.*31A= XP_011527309.1:n.*31A=
XM_011529008.1:c.*31A= XP_011527310.1:n.*31A=
XR_936612.1:n.1526A=
XM_024451971.1:c.1163A= XP_024307739.1:p.Lys388=
NM_003098.3:c.1490A= MANE Select NP_003089.1:p.Lys497=