Canonical Allele Identifier: CA751562934
Gene: SNAP29 HGNC NCBI

Linked Data

dbSNP Id: rs1447422059
gnomAD v3: 22-20888510-C-CA
gnomAD v4: 22-20888510-C-CA
MyVariant Identifiers: chr22:g.21242798_21242799insA (hg19) chr22:g.20888510_20888511insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888511dup , CM000684.2:g.20888511dup GRCh38
NC_000022.10:g.21242799dup , CM000684.1:g.21242799dup GRCh37
NC_000022.9:g.19572799dup NCBI36
NG_012152.1:g.34508dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*675dup MANE Select ENSP00000215730.6:n.*675dup
ENST00000215730.11:c.*675dup ENSP00000215730.6:n.*675dup
NM_004782.3:c.*675dup NP_004773.1:n.*675dup
NM_004782.4:c.*675dup MANE Select NP_004773.1:n.*675dup
Search 100 bp 5'
Search 100 bp 3'