Canonical Allele Identifier: CA2557262665
Gene: SNAP29 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888135dup , CM000684.2:g.20888135dup GRCh38
NC_000022.10:g.21242423dup , CM000684.1:g.21242423dup GRCh37
NC_000022.9:g.19572423dup NCBI36
NG_012152.1:g.34132dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*299dup MANE Select ENSP00000215730.6:n.*299dup
ENST00000215730.11:c.*299dup ENSP00000215730.6:n.*299dup
NM_004782.3:c.*299dup NP_004773.1:n.*299dup
NM_004782.4:c.*299dup MANE Select NP_004773.1:n.*299dup
Search 100 bp 5'
Search 100 bp 3'