Canonical Allele Identifier: CA2396589485
Gene: SNAP29 HGNC NCBI

Linked Data

dbSNP Id: rs1929064586

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888133_20888134del , CM000684.2:g.20888133_20888134del GRCh38
NC_000022.10:g.21242421_21242422del , CM000684.1:g.21242421_21242422del GRCh37
NC_000022.9:g.19572421_19572422del NCBI36
NG_012152.1:g.34130_34131del

Transcript Alleles

HGVS Amino-acid change
ENST00000215730.12:c.*297_*298del MANE Select ENSP00000215730.6:n.*297_*298del
ENST00000215730.11:c.*297_*298del ENSP00000215730.6:n.*297_*298del
NM_004782.3:c.*297_*298del NP_004773.1:n.*297_*298del
NM_004782.4:c.*297_*298del MANE Select NP_004773.1:n.*297_*298del