Canonical Allele Identifier: CA2396589423
Gene: SNAP29 HGNC NCBI

Linked Data

dbSNP Id: rs1929061075

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888018_20888020del , CM000684.2:g.20888018_20888020del GRCh38
NC_000022.10:g.21242306_21242308del , CM000684.1:g.21242306_21242308del GRCh37
NC_000022.9:g.19572306_19572308del NCBI36
NG_012152.1:g.34015_34017del

Transcript Alleles

HGVS Amino-acid change
ENST00000215730.12:c.*182_*184del MANE Select ENSP00000215730.6:n.*182_*184del
ENST00000215730.11:c.*182_*184del ENSP00000215730.6:n.*182_*184del
NM_004782.3:c.*182_*184del NP_004773.1:n.*182_*184del
NM_004782.4:c.*182_*184del MANE Select NP_004773.1:n.*182_*184del