Canonical Allele Identifier: CA2396589600

Gene: SNAP29

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20888337_20888357delinsACACACACACACACACACACT , CM000684.2:g.20888337_20888357delinsACACACACACACACACACACT	GRCh38
NC_000022.10:g.21242625_21242645delinsACACACACACACACACACACT , CM000684.1:g.21242625_21242645delinsACACACACACACACACACACT	GRCh37
NC_000022.9:g.19572625_19572645delinsACACACACACACACACACACT	NCBI36
NG_012152.1:g.34334_34354delinsACACACACACACACACACACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215730.12:c.*501_*521delinsACACACACACACACACACACT MANE Select	ENSP00000215730.6:n.*501_*521delinsACACACACACACACACACACT
ENST00000215730.11:c.*501_*521delinsACACACACACACACACACACT	ENSP00000215730.6:n.*501_*521delinsACACACACACACACACACACT
NM_004782.3:c.*501_*521delinsACACACACACACACACACACT	NP_004773.1:n.*501_*521delinsACACACACACACACACACACT
NM_004782.4:c.*501_*521delinsACACACACACACACACACACT MANE Select	NP_004773.1:n.*501_*521delinsACACACACACACACACACACT