Canonical Allele Identifier: CA751562882
Gene: SNAP29 HGNC NCBI

Linked Data

dbSNP Id: rs886057266
MyVariant Identifiers: chr22:g.21242596_21242607del (hg19) chr22:g.20888308_20888319del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888310_20888321del , CM000684.2:g.20888310_20888321del GRCh38
NC_000022.10:g.21242598_21242609del , CM000684.1:g.21242598_21242609del GRCh37
NC_000022.9:g.19572598_19572609del NCBI36
NG_012152.1:g.34307_34318del

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*474_*485del MANE Select ENSP00000215730.6:n.*474_*485del
ENST00000215730.11:c.*474_*485del ENSP00000215730.6:n.*474_*485del
NM_004782.3:c.*474_*485del NP_004773.1:n.*474_*485del
NM_004782.4:c.*474_*485del MANE Select NP_004773.1:n.*474_*485del
Search 100 bp 5'
Search 100 bp 3'