Canonical Allele Identifier: CA920339310
Gene: SNAP29 HGNC NCBI

Linked Data

dbSNP Id: rs1555915270

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888353_20888357del , CM000684.2:g.20888353_20888357del GRCh38
NC_000022.10:g.21242641_21242645del , CM000684.1:g.21242641_21242645del GRCh37
NC_000022.9:g.19572641_19572645del NCBI36
NG_012152.1:g.34350_34354del

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*517_*521del MANE Select ENSP00000215730.6:n.*517_*521del
ENST00000215730.11:c.*517_*521del ENSP00000215730.6:n.*517_*521del
NM_004782.3:c.*517_*521del NP_004773.1:n.*517_*521del
NM_004782.4:c.*517_*521del MANE Select NP_004773.1:n.*517_*521del