Canonical Allele Identifier: CA1024230540
Gene: SNAP29 HGNC NCBI

Linked Data

dbSNP Id: rs1363748977
gnomAD v3: 22-20888311-T-TCTCACACACACACACA
gnomAD v4: 22-20888311-T-TCTCACACACACACACA
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888312_20888313insTCACACACACACACAC , CM000684.2:g.20888312_20888313insTCACACACACACACAC GRCh38
NC_000022.10:g.21242600_21242601insTCACACACACACACAC , CM000684.1:g.21242600_21242601insTCACACACACACACAC GRCh37
NC_000022.9:g.19572600_19572601insTCACACACACACACAC NCBI36
NG_012152.1:g.34309_34310insTCACACACACACACAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*476_*477insTCACACACACACACAC MANE Select ENSP00000215730.6:n.*476_*477insTCACACACACACACAC
ENST00000215730.11:c.*476_*477insTCACACACACACACAC ENSP00000215730.6:n.*476_*477insTCACACACACACACAC
NM_004782.3:c.*476_*477insTCACACACACACACAC NP_004773.1:n.*476_*477insTCACACACACACACAC
NM_004782.4:c.*476_*477insTCACACACACACACAC MANE Select NP_004773.1:n.*476_*477insTCACACACACACACAC
Search 100 bp 5'
Search 100 bp 3'