Canonical Allele Identifier: CA2396589691

Gene: SNAP29

Linked Data

• dbSNP Id: rs1485902199

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20888477_20888478del , CM000684.2:g.20888477_20888478del	GRCh38
NC_000022.10:g.21242765_21242766del , CM000684.1:g.21242765_21242766del	GRCh37
NC_000022.9:g.19572765_19572766del	NCBI36
NG_012152.1:g.34474_34475del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215730.12:c.*641_*642del MANE Select	ENSP00000215730.6:n.*641_*642del
ENST00000215730.11:c.*641_*642del	ENSP00000215730.6:n.*641_*642del
NM_004782.3:c.*641_*642del	NP_004773.1:n.*641_*642del
NM_004782.4:c.*641_*642del MANE Select	NP_004773.1:n.*641_*642del