Canonical Allele Identifier: CA1024230719
Gene: SNAP29 HGNC NCBI

Linked Data

dbSNP Id: rs1929075746
gnomAD v3: 22-20888378-AT-A
gnomAD v4: 22-20888378-AT-A
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888380del , CM000684.2:g.20888380del GRCh38
NC_000022.10:g.21242668del , CM000684.1:g.21242668del GRCh37
NC_000022.9:g.19572668del NCBI36
NG_012152.1:g.34377del

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*544del MANE Select ENSP00000215730.6:n.*544del
ENST00000215730.11:c.*544del ENSP00000215730.6:n.*544del
NM_004782.3:c.*544del NP_004773.1:n.*544del
NM_004782.4:c.*544del MANE Select NP_004773.1:n.*544del
Search 100 bp 5'
Search 100 bp 3'