Canonical Allele Identifier: CA2396589672

Gene: SNAP29

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20888430_20888437delinsCCATCTTG , CM000684.2:g.20888430_20888437delinsCCATCTTG	GRCh38
NC_000022.10:g.21242718_21242725delinsCCATCTTG , CM000684.1:g.21242718_21242725delinsCCATCTTG	GRCh37
NC_000022.9:g.19572718_19572725delinsCCATCTTG	NCBI36
NG_012152.1:g.34427_34434delinsCCATCTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215730.12:c.*594_*601delinsCCATCTTG MANE Select	ENSP00000215730.6:n.*594_*601delinsCCATCTTG
ENST00000215730.11:c.*594_*601delinsCCATCTTG	ENSP00000215730.6:n.*594_*601delinsCCATCTTG
NM_004782.3:c.*594_*601delinsCCATCTTG	NP_004773.1:n.*594_*601delinsCCATCTTG
NM_004782.4:c.*594_*601delinsCCATCTTG MANE Select	NP_004773.1:n.*594_*601delinsCCATCTTG