Canonical Allele Identifier: CA1024230538
Gene: SNAP29 HGNC NCBI

Linked Data

dbSNP Id: rs1363748977
gnomAD v3: 22-20888311-T-TCTCACACACACACA
gnomAD v4: 22-20888311-T-TCTCACACACACACA
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888312_20888313insTCACACACACACAC , CM000684.2:g.20888312_20888313insTCACACACACACAC GRCh38
NC_000022.10:g.21242600_21242601insTCACACACACACAC , CM000684.1:g.21242600_21242601insTCACACACACACAC GRCh37
NC_000022.9:g.19572600_19572601insTCACACACACACAC NCBI36
NG_012152.1:g.34309_34310insTCACACACACACAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*476_*477insTCACACACACACAC MANE Select ENSP00000215730.6:n.*476_*477insTCACACACACACAC
ENST00000215730.11:c.*476_*477insTCACACACACACAC ENSP00000215730.6:n.*476_*477insTCACACACACACAC
NM_004782.3:c.*476_*477insTCACACACACACAC NP_004773.1:n.*476_*477insTCACACACACACAC
NM_004782.4:c.*476_*477insTCACACACACACAC MANE Select NP_004773.1:n.*476_*477insTCACACACACACAC
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