Canonical Allele Identifier: CA2396589587
Gene: SNAP29 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888323_20888357delinsACACACACACACACACACACACACACACACACACT , CM000684.2:g.20888323_20888357delinsACACACACACACACACACACACACACACACACACT GRCh38
NC_000022.10:g.21242611_21242645delinsACACACACACACACACACACACACACACACACACT , CM000684.1:g.21242611_21242645delinsACACACACACACACACACACACACACACACACACT GRCh37
NC_000022.9:g.19572611_19572645delinsACACACACACACACACACACACACACACACACACT NCBI36
NG_012152.1:g.34320_34354delinsACACACACACACACACACACACACACACACACACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*487_*521delinsACACACACACACACACACACACACACACACACACT MANE Select ENSP00000215730.6:n.*487_*521delinsACACACACACACACACACACACACAC...
ENST00000215730.11:c.*487_*521delinsACACACACACACACACACACACACACACACACACT ENSP00000215730.6:n.*487_*521delinsACACACACACACACACACACACACAC...
NM_004782.3:c.*487_*521delinsACACACACACACACACACACACACACACACACACT NP_004773.1:n.*487_*521delinsACACACACACACACACACACACACACACACAC...
NM_004782.4:c.*487_*521delinsACACACACACACACACACACACACACACACACACT MANE Select NP_004773.1:n.*487_*521delinsACACACACACACACACACACACACACACACAC...