Canonical Allele Identifier: CA2396589565
Gene: SNAP29 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888310_20888315delinsTTCACA , CM000684.2:g.20888310_20888315delinsTTCACA GRCh38
NC_000022.10:g.21242598_21242603delinsTTCACA , CM000684.1:g.21242598_21242603delinsTTCACA GRCh37
NC_000022.9:g.19572598_19572603delinsTTCACA NCBI36
NG_012152.1:g.34307_34312delinsTTCACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*474_*479delinsTTCACA MANE Select ENSP00000215730.6:n.*474_*479delinsTTCACA
ENST00000215730.11:c.*474_*479delinsTTCACA ENSP00000215730.6:n.*474_*479delinsTTCACA
NM_004782.3:c.*474_*479delinsTTCACA NP_004773.1:n.*474_*479delinsTTCACA
NM_004782.4:c.*474_*479delinsTTCACA MANE Select NP_004773.1:n.*474_*479delinsTTCACA