Canonical Allele Identifier: CA2396589690

Gene: SNAP29

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20888472_20888474delinsGCC , CM000684.2:g.20888472_20888474delinsGCC	GRCh38
NC_000022.10:g.21242760_21242762delinsGCC , CM000684.1:g.21242760_21242762delinsGCC	GRCh37
NC_000022.9:g.19572760_19572762delinsGCC	NCBI36
NG_012152.1:g.34469_34471delinsGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215730.12:c.*636_*638delinsGCC MANE Select	ENSP00000215730.6:n.*636_*638delinsGCC
ENST00000215730.11:c.*636_*638delinsGCC	ENSP00000215730.6:n.*636_*638delinsGCC
NM_004782.3:c.*636_*638delinsGCC	NP_004773.1:n.*636_*638delinsGCC
NM_004782.4:c.*636_*638delinsGCC MANE Select	NP_004773.1:n.*636_*638delinsGCC