Canonical Allele Identifier: CA1024230406
Gene: SNAP29 HGNC NCBI

Linked Data

dbSNP Id: rs1929065334
gnomAD v3: 22-20888175-G-GA
gnomAD v4: 22-20888175-G-GA
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888177dup , CM000684.2:g.20888177dup GRCh38
NC_000022.10:g.21242465dup , CM000684.1:g.21242465dup GRCh37
NC_000022.9:g.19572465dup NCBI36
NG_012152.1:g.34174dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*341dup MANE Select ENSP00000215730.6:n.*341dup
ENST00000215730.11:c.*341dup ENSP00000215730.6:n.*341dup
NM_004782.3:c.*341dup NP_004773.1:n.*341dup
NM_004782.4:c.*341dup MANE Select NP_004773.1:n.*341dup
Search 100 bp 5'
Search 100 bp 3'