Canonical Allele Identifier: CA2360755105
Gene: SNTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33443712G= , CM000682.2:g.33443712G= GRCh38
NC_000020.10:g.32031518G= , CM000682.1:g.32031518G= GRCh37
NC_000020.9:g.31495179G= NCBI36
NG_011622.1:g.5181C= , LRG_332:g.5181C=

Transcript Alleles

HGVS Amino-acid change
ENST00000217381.3:c.-92C= MANE Select ENSP00000217381.2:n.-92C=
ENST00000217381.2:c.-92C= ENSP00000217381.2:n.-92C=
NM_003098.2:c.-92C= , LRG_332t1:c.-92C= NP_003089.1:n.-92C=
XM_005260517.1:c.-92C= XP_005260574.1:n.-92C=
XM_011529007.1:c.-92C= XP_011527309.1:n.-92C=
XM_011529008.1:c.-92C= XP_011527310.1:n.-92C=
XR_936612.1:n.142C=
NM_003098.3:c.-92C= MANE Select NP_003089.1:n.-92C=