Canonical Allele Identifier: CA2655449509
Gene: SNAP29 HGNC NCBI

Linked Data

gnomAD v4: 22-20888472-GC-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888478del , CM000684.2:g.20888478del GRCh38
NC_000022.10:g.21242766del , CM000684.1:g.21242766del GRCh37
NC_000022.9:g.19572766del NCBI36
NG_012152.1:g.34475del

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*642del MANE Select ENSP00000215730.6:n.*642del
ENST00000215730.11:c.*642del ENSP00000215730.6:n.*642del
NM_004782.3:c.*642del NP_004773.1:n.*642del
NM_004782.4:c.*642del MANE Select NP_004773.1:n.*642del
Search 100 bp 5'
Search 100 bp 3'