Canonical Allele Identifier: CA2818431151
Gene: SNAP29 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888133T>G , CM000684.2:g.20888133T>G GRCh38
NC_000022.10:g.21242421T>G , CM000684.1:g.21242421T>G GRCh37
NC_000022.9:g.19572421T>G NCBI36
NG_012152.1:g.34130T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*297T>G MANE Select ENSP00000215730.6:n.*297T>G
ENST00000215730.11:c.*297T>G ENSP00000215730.6:n.*297T>G
NM_004782.3:c.*297T>G NP_004773.1:n.*297T>G
NM_004782.4:c.*297T>G MANE Select NP_004773.1:n.*297T>G
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