Canonical Allele Identifier: CA2396589433

Gene: SNAP29

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20888040_20888041delinsTC , CM000684.2:g.20888040_20888041delinsTC	GRCh38
NC_000022.10:g.21242328_21242329delinsTC , CM000684.1:g.21242328_21242329delinsTC	GRCh37
NC_000022.9:g.19572328_19572329delinsTC	NCBI36
NG_012152.1:g.34037_34038delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215730.12:c.*204_*205delinsTC MANE Select	ENSP00000215730.6:n.*204_*205delinsTC
ENST00000215730.11:c.*204_*205delinsTC	ENSP00000215730.6:n.*204_*205delinsTC
NM_004782.3:c.*204_*205delinsTC	NP_004773.1:n.*204_*205delinsTC
NM_004782.4:c.*204_*205delinsTC MANE Select	NP_004773.1:n.*204_*205delinsTC