Canonical Allele Identifier: CA751562883
Gene: SNAP29 HGNC NCBI

Linked Data

dbSNP Id: rs1171630471
gnomAD v4: 22-20888309-ATT-A
MyVariant Identifiers: chr22:g.21242598_21242599del (hg19) chr22:g.20888310_20888311del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888310_20888311del , CM000684.2:g.20888310_20888311del GRCh38
NC_000022.10:g.21242598_21242599del , CM000684.1:g.21242598_21242599del GRCh37
NC_000022.9:g.19572598_19572599del NCBI36
NG_012152.1:g.34307_34308del

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*474_*475del MANE Select ENSP00000215730.6:n.*474_*475del
ENST00000215730.11:c.*474_*475del ENSP00000215730.6:n.*474_*475del
NM_004782.3:c.*474_*475del NP_004773.1:n.*474_*475del
NM_004782.4:c.*474_*475del MANE Select NP_004773.1:n.*474_*475del
Search 100 bp 5'
Search 100 bp 3'