Canonical Allele Identifier: CA322277428
Gene: SNAP29 HGNC NCBI

Linked Data

dbSNP Id: rs759793507
MyVariant Identifiers: chr22:g.21242249del (hg19) chr22:g.20887961del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20887961del , CM000684.2:g.20887961del GRCh38
NC_000022.10:g.21242249del , CM000684.1:g.21242249del GRCh37
NC_000022.9:g.19572249del NCBI36
NG_012152.1:g.33958del

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*125del MANE Select ENSP00000215730.6:n.*125del
ENST00000215730.11:c.*125del ENSP00000215730.6:n.*125del
NM_004782.3:c.*125del NP_004773.1:n.*125del
NM_004782.4:c.*125del MANE Select NP_004773.1:n.*125del
Search 100 bp 5'
Search 100 bp 3'