Canonical Allele Identifier: CA322277698
Gene: SNAP29 HGNC NCBI

Linked Data

dbSNP Id: rs757531727
MyVariant Identifiers: chr22:g.21242634_21242636del (hg19) chr22:g.20888346_20888348del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888346_20888348del , CM000684.2:g.20888346_20888348del GRCh38
NC_000022.10:g.21242634_21242636del , CM000684.1:g.21242634_21242636del GRCh37
NC_000022.9:g.19572634_19572636del NCBI36
NG_012152.1:g.34343_34345del

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*510_*512del MANE Select ENSP00000215730.6:n.*510_*512del
ENST00000215730.11:c.*510_*512del ENSP00000215730.6:n.*510_*512del
NM_004782.3:c.*510_*512del NP_004773.1:n.*510_*512del
NM_004782.4:c.*510_*512del MANE Select NP_004773.1:n.*510_*512del
Search 100 bp 5'
Search 100 bp 3'