Canonical Allele Identifier: CA2396589568

Gene: SNAP29

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20888310_20888322delinsTTCACACACACAC , CM000684.2:g.20888310_20888322delinsTTCACACACACAC	GRCh38
NC_000022.10:g.21242598_21242610delinsTTCACACACACAC , CM000684.1:g.21242598_21242610delinsTTCACACACACAC	GRCh37
NC_000022.9:g.19572598_19572610delinsTTCACACACACAC	NCBI36
NG_012152.1:g.34307_34319delinsTTCACACACACAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215730.12:c.*474_*486delinsTTCACACACACAC MANE Select	ENSP00000215730.6:n.*474_*486delinsTTCACACACACAC
ENST00000215730.11:c.*474_*486delinsTTCACACACACAC	ENSP00000215730.6:n.*474_*486delinsTTCACACACACAC
NM_004782.3:c.*474_*486delinsTTCACACACACAC	NP_004773.1:n.*474_*486delinsTTCACACACACAC
NM_004782.4:c.*474_*486delinsTTCACACACACAC MANE Select	NP_004773.1:n.*474_*486delinsTTCACACACACAC