Canonical Allele Identifier: CA2396589619

Gene: SNAP29

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20888347_20888357delinsACACACACACT , CM000684.2:g.20888347_20888357delinsACACACACACT	GRCh38
NC_000022.10:g.21242635_21242645delinsACACACACACT , CM000684.1:g.21242635_21242645delinsACACACACACT	GRCh37
NC_000022.9:g.19572635_19572645delinsACACACACACT	NCBI36
NG_012152.1:g.34344_34354delinsACACACACACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215730.12:c.*511_*521delinsACACACACACT MANE Select	ENSP00000215730.6:n.*511_*521delinsACACACACACT
ENST00000215730.11:c.*511_*521delinsACACACACACT	ENSP00000215730.6:n.*511_*521delinsACACACACACT
NM_004782.3:c.*511_*521delinsACACACACACT	NP_004773.1:n.*511_*521delinsACACACACACT
NM_004782.4:c.*511_*521delinsACACACACACT MANE Select	NP_004773.1:n.*511_*521delinsACACACACACT