Canonical Allele Identifier: CA2652478411

Gene: SNTA1

Linked Data

• gnomAD v4: 20-33443557-CCG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33443558_33443559del , CM000682.2:g.33443558_33443559del	GRCh38
NC_000020.10:g.32031364_32031365del , CM000682.1:g.32031364_32031365del	GRCh37
NC_000020.9:g.31495025_31495026del	NCBI36
NG_011622.1:g.5334_5335del , LRG_332:g.5334_5335del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.62_63del MANE Select	ENSP00000217381.2:p.Ser21TrpfsTer?
ENST00000217381.2:c.62_63del	ENSP00000217381.2:p.Ser21TrpfsTer?
NM_003098.2:c.62_63del , LRG_332t1:c.62_63del	NP_003089.1:p.Ser21TrpfsTer?
XM_005260517.1:c.62_63del	XP_005260574.1:p.Ser21TrpfsTer?
XM_011529007.1:c.62_63del	XP_011527309.1:p.Ser21TrpfsTer?
XM_011529008.1:c.62_63del	XP_011527310.1:p.Ser21TrpfsTer?
XR_936612.1:n.295_296del
NM_003098.3:c.62_63del MANE Select	NP_003089.1:p.Ser21TrpfsTer?