Canonical Allele Identifier: CA1024230479
Gene: SNAP29 HGNC NCBI

Linked Data

dbSNP Id: rs1929068802

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888310_20888311insACACACAC , CM000684.2:g.20888310_20888311insACACACAC GRCh38
NC_000022.10:g.21242598_21242599insACACACAC , CM000684.1:g.21242598_21242599insACACACAC GRCh37
NC_000022.9:g.19572598_19572599insACACACAC NCBI36
NG_012152.1:g.34307_34308insACACACAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*474_*475insACACACAC MANE Select ENSP00000215730.6:n.*474_*475insACACACAC
ENST00000215730.11:c.*474_*475insACACACAC ENSP00000215730.6:n.*474_*475insACACACAC
NM_004782.3:c.*474_*475insACACACAC NP_004773.1:n.*474_*475insACACACAC
NM_004782.4:c.*474_*475insACACACAC MANE Select NP_004773.1:n.*474_*475insACACACAC