Canonical Allele Identifier: CA751562903
Gene: SNAP29 HGNC NCBI

Linked Data

dbSNP Id: rs1363748977
gnomAD v3: 22-20888311-T-TCTCACACACACA
gnomAD v4: 22-20888311-T-TCTCACACACACA
MyVariant Identifiers: chr22:g.21242599_21242600insCTCACACACACA (hg19) chr22:g.20888311_20888312insCTCACACACACA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888312_20888313insTCACACACACAC , CM000684.2:g.20888312_20888313insTCACACACACAC GRCh38
NC_000022.10:g.21242600_21242601insTCACACACACAC , CM000684.1:g.21242600_21242601insTCACACACACAC GRCh37
NC_000022.9:g.19572600_19572601insTCACACACACAC NCBI36
NG_012152.1:g.34309_34310insTCACACACACAC

Transcript Alleles

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