Canonical Allele Identifier: CA2652478423
Gene: SNTA1 HGNC NCBI

Linked Data

gnomAD v4: 20-33443597-C-CG
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33443601dup , CM000682.2:g.33443601dup GRCh38
NC_000020.10:g.32031407dup , CM000682.1:g.32031407dup GRCh37
NC_000020.9:g.31495068dup NCBI36
NG_011622.1:g.5295dup , LRG_332:g.5295dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.3:c.23dup MANE Select ENSP00000217381.2:p.Arg9AlafsTer?
ENST00000217381.2:c.23dup ENSP00000217381.2:p.Arg9AlafsTer?
NM_003098.2:c.23dup , LRG_332t1:c.23dup NP_003089.1:p.Arg9AlafsTer?
XM_005260517.1:c.23dup XP_005260574.1:p.Arg9AlafsTer?
XM_011529007.1:c.23dup XP_011527309.1:p.Arg9AlafsTer?
XM_011529008.1:c.23dup XP_011527310.1:p.Arg9AlafsTer?
XR_936612.1:n.256dup
NM_003098.3:c.23dup MANE Select NP_003089.1:p.Arg9AlafsTer?
Search 100 bp 5'
Search 100 bp 3'