Canonical Allele Identifier: CA982856622
Gene: SLC6A4 HGNC NCBI

Linked Data

dbSNP Id: rs1906752098
gnomAD v3: 17-30221459-CCCCAGGTCACAGCCCACCCGGGTCACAGCCCAT-C
gnomAD v4: 17-30221459-CCCCAGGTCACAGCCCACCCGGGTCACAGCCCAT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30221479_30221511del , CM000679.2:g.30221479_30221511del GRCh38
NC_000017.10:g.28548497_28548529del , CM000679.1:g.28548497_28548529del GRCh37
NC_000017.9:g.25572623_25572655del NCBI36
NG_011747.2:g.19445_19477del

Transcript Alleles

HGVS Amino-acid Change
ENST00000650711.1:c.343+124_343+156del MANE Select ENSP00000498537.1:n.343+124_343+156del
ENST00000261707.7:c.343+124_343+156del ENSP00000261707.3:n.343+124_343+156del
ENST00000394821.2:c.343+124_343+156del ENSP00000378298.2:n.343+124_343+156del
ENST00000401766.6:c.343+124_343+156del ENSP00000385822.2:n.343+124_343+156del
NM_001045.5:c.343+124_343+156del NP_001036.1:n.343+124_343+156del
NM_001045.6:c.343+124_343+156del MANE Select NP_001036.1:n.343+124_343+156del
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