Canonical Allele Identifier: CA2360755027
Gene: SNTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33443598G= , CM000682.2:g.33443598G= GRCh38
NC_000020.10:g.32031404G= , CM000682.1:g.32031404G= GRCh37
NC_000020.9:g.31495065G= NCBI36
NG_011622.1:g.5295C= , LRG_332:g.5295C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.3:c.23C= MANE Select ENSP00000217381.2:p.Pro8=
ENST00000217381.2:c.23C= ENSP00000217381.2:p.Pro8=
NM_003098.2:c.23C= , LRG_332t1:c.23C= NP_003089.1:p.Pro8=
XM_005260517.1:c.23C= XP_005260574.1:p.Pro8=
XM_011529007.1:c.23C= XP_011527309.1:p.Pro8=
XM_011529008.1:c.23C= XP_011527310.1:p.Pro8=
XR_936612.1:n.256C=
NM_003098.3:c.23C= MANE Select NP_003089.1:p.Pro8=