Canonical Allele Identifier: CA2396589598

Gene: SNAP29

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20888335_20888357delinsACACACACACACACACACACACT , CM000684.2:g.20888335_20888357delinsACACACACACACACACACACACT	GRCh38
NC_000022.10:g.21242623_21242645delinsACACACACACACACACACACACT , CM000684.1:g.21242623_21242645delinsACACACACACACACACACACACT	GRCh37
NC_000022.9:g.19572623_19572645delinsACACACACACACACACACACACT	NCBI36
NG_012152.1:g.34332_34354delinsACACACACACACACACACACACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215730.12:c.*499_*521delinsACACACACACACACACACACACT MANE Select	ENSP00000215730.6:n.*499_*521delinsACACACACACACACACACACACT
ENST00000215730.11:c.*499_*521delinsACACACACACACACACACACACT	ENSP00000215730.6:n.*499_*521delinsACACACACACACACACACACACT
NM_004782.3:c.*499_*521delinsACACACACACACACACACACACT	NP_004773.1:n.*499_*521delinsACACACACACACACACACACACT
NM_004782.4:c.*499_*521delinsACACACACACACACACACACACT MANE Select	NP_004773.1:n.*499_*521delinsACACACACACACACACACACACT