Canonical Allele Identifier: CA2655449263
Gene: SNAP29 HGNC NCBI

Linked Data

gnomAD v4: 22-20888215-CT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888216del , CM000684.2:g.20888216del GRCh38
NC_000022.10:g.21242504del , CM000684.1:g.21242504del GRCh37
NC_000022.9:g.19572504del NCBI36
NG_012152.1:g.34213del

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*380del MANE Select ENSP00000215730.6:n.*380del
ENST00000215730.11:c.*380del ENSP00000215730.6:n.*380del
NM_004782.3:c.*380del NP_004773.1:n.*380del
NM_004782.4:c.*380del MANE Select NP_004773.1:n.*380del
Search 100 bp 5'
Search 100 bp 3'