Canonical Allele Identifier: CA2396589588
Gene: SNAP29 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888325_20888357delinsACACACACACACACACACACACACACACACACT , CM000684.2:g.20888325_20888357delinsACACACACACACACACACACACACACACACACT GRCh38
NC_000022.10:g.21242613_21242645delinsACACACACACACACACACACACACACACACACT , CM000684.1:g.21242613_21242645delinsACACACACACACACACACACACACACACACACT GRCh37
NC_000022.9:g.19572613_19572645delinsACACACACACACACACACACACACACACACACT NCBI36
NG_012152.1:g.34322_34354delinsACACACACACACACACACACACACACACACACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*489_*521delinsACACACACACACACACACACACACACACACACT MANE Select ENSP00000215730.6:n.*489_*521delinsACACACACACACACACACACACACAC...
ENST00000215730.11:c.*489_*521delinsACACACACACACACACACACACACACACACACT ENSP00000215730.6:n.*489_*521delinsACACACACACACACACACACACACAC...
NM_004782.3:c.*489_*521delinsACACACACACACACACACACACACACACACACT NP_004773.1:n.*489_*521delinsACACACACACACACACACACACACACACACAC...
NM_004782.4:c.*489_*521delinsACACACACACACACACACACACACACACACACT MANE Select NP_004773.1:n.*489_*521delinsACACACACACACACACACACACACACACACAC...