Canonical Allele Identifier: CA2396589564

Gene: SNAP29

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20888310_20888312delinsTTC , CM000684.2:g.20888310_20888312delinsTTC	GRCh38
NC_000022.10:g.21242598_21242600delinsTTC , CM000684.1:g.21242598_21242600delinsTTC	GRCh37
NC_000022.9:g.19572598_19572600delinsTTC	NCBI36
NG_012152.1:g.34307_34309delinsTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215730.12:c.*474_*476delinsTTC MANE Select	ENSP00000215730.6:n.*474_*476delinsTTC
ENST00000215730.11:c.*474_*476delinsTTC	ENSP00000215730.6:n.*474_*476delinsTTC
NM_004782.3:c.*474_*476delinsTTC	NP_004773.1:n.*474_*476delinsTTC
NM_004782.4:c.*474_*476delinsTTC MANE Select	NP_004773.1:n.*474_*476delinsTTC