Canonical Allele Identifier: CA2655449236

Gene: SNAP29

Linked Data

• gnomAD v4: 22-20888124-TAAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20888129_20888131del , CM000684.2:g.20888129_20888131del	GRCh38
NC_000022.10:g.21242417_21242419del , CM000684.1:g.21242417_21242419del	GRCh37
NC_000022.9:g.19572417_19572419del	NCBI36
NG_012152.1:g.34126_34128del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215730.12:c.*293_*295del MANE Select	ENSP00000215730.6:n.*293_*295del
ENST00000215730.11:c.*293_*295del	ENSP00000215730.6:n.*293_*295del
NM_004782.3:c.*293_*295del	NP_004773.1:n.*293_*295del
NM_004782.4:c.*293_*295del MANE Select	NP_004773.1:n.*293_*295del