Canonical Allele Identifier: CA2738111779
Gene: SNAP29 HGNC NCBI

Linked Data

dbSNP Id: rs2147875180

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888319_20888320insTG , CM000684.2:g.20888319_20888320insTG GRCh38
NC_000022.10:g.21242607_21242608insTG , CM000684.1:g.21242607_21242608insTG GRCh37
NC_000022.9:g.19572607_19572608insTG NCBI36
NG_012152.1:g.34316_34317insTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*483_*484insTG MANE Select ENSP00000215730.6:n.*483_*484insTG
ENST00000215730.11:c.*483_*484insTG ENSP00000215730.6:n.*483_*484insTG
NM_004782.3:c.*483_*484insTG NP_004773.1:n.*483_*484insTG
NM_004782.4:c.*483_*484insTG MANE Select NP_004773.1:n.*483_*484insTG