Canonical Allele Identifier: CA2396589474
Gene: SNAP29 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888104G= , CM000684.2:g.20888104G= GRCh38
NC_000022.10:g.21242392G= , CM000684.1:g.21242392G= GRCh37
NC_000022.9:g.19572392G= NCBI36
NG_012152.1:g.34101G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*268G= MANE Select ENSP00000215730.6:n.*268G=
ENST00000215730.11:c.*268G= ENSP00000215730.6:n.*268G=
NM_004782.3:c.*268G= NP_004773.1:n.*268G=
NM_004782.4:c.*268G= MANE Select NP_004773.1:n.*268G=
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