Canonical Allele Identifier: CA1024230578
Gene: SNAP29 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888356_20888357insACACACACACACACACACACACACACACACACACACACACACACAC , CM000684.2:g.20888356_20888357insACACACACACACACACACACACACACACACACACACACACACACAC GRCh38
NC_000022.10:g.21242644_21242645insACACACACACACACACACACACACACACACACACACACACACACAC , CM000684.1:g.21242644_21242645insACACACACACACACACACACACACACACACACACACACACACACAC GRCh37
NC_000022.9:g.19572644_19572645insACACACACACACACACACACACACACACACACACACACACACACAC NCBI36
NG_012152.1:g.34353_34354insACACACACACACACACACACACACACACACACACACACACACACAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*520_*521insACACACACACACACACACACACACACACACACACACACACACACAC MANE Select ENSP00000215730.6:n.*520_*521insACACACACACACACACACACACACACACA...
ENST00000215730.11:c.*520_*521insACACACACACACACACACACACACACACACACACACACACACACAC ENSP00000215730.6:n.*520_*521insACACACACACACACACACACACACACACA...
NM_004782.3:c.*520_*521insACACACACACACACACACACACACACACACACACACACACACACAC NP_004773.1:n.*520_*521insACACACACACACACACACACACACACACACACACA...
NM_004782.4:c.*520_*521insACACACACACACACACACACACACACACACACACACACACACACAC MANE Select NP_004773.1:n.*520_*521insACACACACACACACACACACACACACACACACACA...