Canonical Allele Identifier: CA2655449251

Gene: SNAP29

Linked Data

• gnomAD v4: 22-20888173-CAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20888175_20888176del , CM000684.2:g.20888175_20888176del	GRCh38
NC_000022.10:g.21242463_21242464del , CM000684.1:g.21242463_21242464del	GRCh37
NC_000022.9:g.19572463_19572464del	NCBI36
NG_012152.1:g.34172_34173del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215730.12:c.*339_*340del MANE Select	ENSP00000215730.6:n.*339_*340del
ENST00000215730.11:c.*339_*340del	ENSP00000215730.6:n.*339_*340del
NM_004782.3:c.*339_*340del	NP_004773.1:n.*339_*340del
NM_004782.4:c.*339_*340del MANE Select	NP_004773.1:n.*339_*340del