Canonical Allele Identifier: CA920339314

Gene: SNAP29

Linked Data

• dbSNP Id: rs1569122334
• gnomAD v4: 22-20888517-GCACTGCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20888524_20888530del , CM000684.2:g.20888524_20888530del	GRCh38
NC_000022.10:g.21242812_21242818del , CM000684.1:g.21242812_21242818del	GRCh37
NC_000022.9:g.19572812_19572818del	NCBI36
NG_012152.1:g.34521_34527del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215730.12:c.*688_*694del MANE Select	ENSP00000215730.6:n.*688_*694del
ENST00000215730.11:c.*688_*694del	ENSP00000215730.6:n.*688_*694del
NM_004782.3:c.*688_*694del	NP_004773.1:n.*688_*694del
NM_004782.4:c.*688_*694del MANE Select	NP_004773.1:n.*688_*694del