Canonical Allele Identifier: CA2655449248
Gene: SNAP29 HGNC NCBI

Linked Data

gnomAD v4: 22-20888167-TG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888170del , CM000684.2:g.20888170del GRCh38
NC_000022.10:g.21242458del , CM000684.1:g.21242458del GRCh37
NC_000022.9:g.19572458del NCBI36
NG_012152.1:g.34167del

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*334del MANE Select ENSP00000215730.6:n.*334del
ENST00000215730.11:c.*334del ENSP00000215730.6:n.*334del
NM_004782.3:c.*334del NP_004773.1:n.*334del
NM_004782.4:c.*334del MANE Select NP_004773.1:n.*334del
Search 100 bp 5'
Search 100 bp 3'