Canonical Allele Identifier: CA2396589638

Gene: SNAP29

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20888358_20888362delinsCTCTG , CM000684.2:g.20888358_20888362delinsCTCTG	GRCh38
NC_000022.10:g.21242646_21242650delinsCTCTG , CM000684.1:g.21242646_21242650delinsCTCTG	GRCh37
NC_000022.9:g.19572646_19572650delinsCTCTG	NCBI36
NG_012152.1:g.34355_34359delinsCTCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215730.12:c.*522_*526delinsCTCTG MANE Select	ENSP00000215730.6:n.*522_*526delinsCTCTG
ENST00000215730.11:c.*522_*526delinsCTCTG	ENSP00000215730.6:n.*522_*526delinsCTCTG
NM_004782.3:c.*522_*526delinsCTCTG	NP_004773.1:n.*522_*526delinsCTCTG
NM_004782.4:c.*522_*526delinsCTCTG MANE Select	NP_004773.1:n.*522_*526delinsCTCTG