Canonical Allele Identifier: CA2396589611

Gene: SNAP29

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20888342_20888343delinsCA , CM000684.2:g.20888342_20888343delinsCA	GRCh38
NC_000022.10:g.21242630_21242631delinsCA , CM000684.1:g.21242630_21242631delinsCA	GRCh37
NC_000022.9:g.19572630_19572631delinsCA	NCBI36
NG_012152.1:g.34339_34340delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215730.12:c.*506_*507delinsCA MANE Select	ENSP00000215730.6:n.*506_*507delinsCA
ENST00000215730.11:c.*506_*507delinsCA	ENSP00000215730.6:n.*506_*507delinsCA
NM_004782.3:c.*506_*507delinsCA	NP_004773.1:n.*506_*507delinsCA
NM_004782.4:c.*506_*507delinsCA MANE Select	NP_004773.1:n.*506_*507delinsCA