Canonical Allele Identifier: CA2396589701

Gene: SNAP29

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20888490_20888495delinsGTATAT , CM000684.2:g.20888490_20888495delinsGTATAT	GRCh38
NC_000022.10:g.21242778_21242783delinsGTATAT , CM000684.1:g.21242778_21242783delinsGTATAT	GRCh37
NC_000022.9:g.19572778_19572783delinsGTATAT	NCBI36
NG_012152.1:g.34487_34492delinsGTATAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215730.12:c.*654_*659delinsGTATAT MANE Select	ENSP00000215730.6:n.*654_*659delinsGTATAT
ENST00000215730.11:c.*654_*659delinsGTATAT	ENSP00000215730.6:n.*654_*659delinsGTATAT
NM_004782.3:c.*654_*659delinsGTATAT	NP_004773.1:n.*654_*659delinsGTATAT
NM_004782.4:c.*654_*659delinsGTATAT MANE Select	NP_004773.1:n.*654_*659delinsGTATAT