Canonical Allele Identifier: CA2396589695
Gene: SNAP29 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888477C= , CM000684.2:g.20888477C= GRCh38
NC_000022.10:g.21242765C= , CM000684.1:g.21242765C= GRCh37
NC_000022.9:g.19572765C= NCBI36
NG_012152.1:g.34474C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*641C= MANE Select ENSP00000215730.6:n.*641C=
ENST00000215730.11:c.*641C= ENSP00000215730.6:n.*641C=
NM_004782.3:c.*641C= NP_004773.1:n.*641C=
NM_004782.4:c.*641C= MANE Select NP_004773.1:n.*641C=
Search 100 bp 5'
Search 100 bp 3'