Canonical Allele Identifier: CA2396590063
Gene: SNAP29 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20889368T= , CM000684.2:g.20889368T= GRCh38
NC_000022.10:g.21243656T= , CM000684.1:g.21243656T= GRCh37
NC_000022.9:g.19573656T= NCBI36
NG_012152.1:g.35365T=

Transcript Alleles

HGVS Amino-acid change
ENST00000215730.12:c.*1532T= MANE Select ENSP00000215730.6:n.*1532T=
ENST00000215730.11:c.*1532T= ENSP00000215730.6:n.*1532T=
NM_004782.3:c.*1532T= NP_004773.1:n.*1532T=
NM_004782.4:c.*1532T= MANE Select NP_004773.1:n.*1532T=
Search 100 bp 5'
Search 100 bp 3'