Canonical Allele Identifier: CA1024230701

Gene: SNAP29

Linked Data

• gnomAD v3: 22-20888360-CTG-C
• gnomAD v4: 22-20888360-CTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20888361_20888362del , CM000684.2:g.20888361_20888362del	GRCh38
NC_000022.10:g.21242649_21242650del , CM000684.1:g.21242649_21242650del	GRCh37
NC_000022.9:g.19572649_19572650del	NCBI36
NG_012152.1:g.34358_34359del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215730.12:c.*525_*526del MANE Select	ENSP00000215730.6:n.*525_*526del
ENST00000215730.11:c.*525_*526del	ENSP00000215730.6:n.*525_*526del
NM_004782.3:c.*525_*526del	NP_004773.1:n.*525_*526del
NM_004782.4:c.*525_*526del MANE Select	NP_004773.1:n.*525_*526del