Canonical Allele Identifier: CA982856648
Gene: SLC6A4 HGNC NCBI

Linked Data

dbSNP Id: rs1906752881
gnomAD v3: 17-30221468-ACAGCCCACCCGGGTCACAGCCCATCCCAGGTCACAGCCCACCCCAGGTCG-A
gnomAD v4: 17-30221468-ACAGCCCACCCGGGTCACAGCCCATCCCAGGTCACAGCCCACCCCAGGTCG-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30221492_30221541del , CM000679.2:g.30221492_30221541del GRCh38
NC_000017.10:g.28548510_28548559del , CM000679.1:g.28548510_28548559del GRCh37
NC_000017.9:g.25572636_25572685del NCBI36
NG_011747.2:g.19419_19468del

Transcript Alleles

HGVS Amino-acid Change
ENST00000650711.1:c.343+98_343+147del MANE Select ENSP00000498537.1:n.343+98_343+147del
ENST00000261707.7:c.343+98_343+147del ENSP00000261707.3:n.343+98_343+147del
ENST00000394821.2:c.343+98_343+147del ENSP00000378298.2:n.343+98_343+147del
ENST00000401766.6:c.343+98_343+147del ENSP00000385822.2:n.343+98_343+147del
NM_001045.5:c.343+98_343+147del NP_001036.1:n.343+98_343+147del
NM_001045.6:c.343+98_343+147del MANE Select NP_001036.1:n.343+98_343+147del
Search 100 bp 5'
Search 100 bp 3'