Canonical Allele Identifier: CA2396589595
Gene: SNAP29 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888331_20888357delinsACACACACACACACACACACACACACT , CM000684.2:g.20888331_20888357delinsACACACACACACACACACACACACACT GRCh38
NC_000022.10:g.21242619_21242645delinsACACACACACACACACACACACACACT , CM000684.1:g.21242619_21242645delinsACACACACACACACACACACACACACT GRCh37
NC_000022.9:g.19572619_19572645delinsACACACACACACACACACACACACACT NCBI36
NG_012152.1:g.34328_34354delinsACACACACACACACACACACACACACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*495_*521delinsACACACACACACACACACACACACACT MANE Select ENSP00000215730.6:n.*495_*521delinsACACACACACACACACACACACACAC...
ENST00000215730.11:c.*495_*521delinsACACACACACACACACACACACACACT ENSP00000215730.6:n.*495_*521delinsACACACACACACACACACACACACAC...
NM_004782.3:c.*495_*521delinsACACACACACACACACACACACACACT NP_004773.1:n.*495_*521delinsACACACACACACACACACACACACACT
NM_004782.4:c.*495_*521delinsACACACACACACACACACACACACACT MANE Select NP_004773.1:n.*495_*521delinsACACACACACACACACACACACACACT