Canonical Allele Identifier: CA2360740078
Gene: SNTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33408538G= , CM000682.2:g.33408538G= GRCh38
NC_000020.10:g.31996344G= , CM000682.1:g.31996344G= GRCh37
NC_000020.9:g.31460005G= NCBI36
NG_011622.1:g.40355C= , LRG_332:g.40355C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.3:c.1487C= MANE Select ENSP00000217381.2:p.Ala496=
ENST00000217381.2:c.1487C= ENSP00000217381.2:p.Ala496=
NM_003098.2:c.1487C= , LRG_332t1:c.1487C= NP_003089.1:p.Ala496=
XM_005260517.1:c.1484C= XP_005260574.1:p.Ala495=
XM_011529007.1:c.*28C= XP_011527309.1:n.*28C=
XM_011529008.1:c.*28C= XP_011527310.1:n.*28C=
XR_936612.1:n.1523C=
XM_024451971.1:c.1160C= XP_024307739.1:p.Ala387=
NM_003098.3:c.1487C= MANE Select NP_003089.1:p.Ala496=