Canonical Allele Identifier: CA2818431283
Gene: SNAP29 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888523del , CM000684.2:g.20888523del GRCh38
NC_000022.10:g.21242811del , CM000684.1:g.21242811del GRCh37
NC_000022.9:g.19572811del NCBI36
NG_012152.1:g.34520del

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*687del MANE Select ENSP00000215730.6:n.*687del
ENST00000215730.11:c.*687del ENSP00000215730.6:n.*687del
NM_004782.3:c.*687del NP_004773.1:n.*687del
NM_004782.4:c.*687del MANE Select NP_004773.1:n.*687del
Search 100 bp 5'
Search 100 bp 3'