Canonical Allele Identifier: CA982856518
Gene: SLC6A4 HGNC NCBI

Linked Data

gnomAD v3: 17-30221412-C-CT
gnomAD v4: 17-30221412-C-CT
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30221412_30221413insT , CM000679.2:g.30221412_30221413insT GRCh38
NC_000017.10:g.28548430_28548431insT , CM000679.1:g.28548430_28548431insT GRCh37
NC_000017.9:g.25572556_25572557insT NCBI36
NG_011747.2:g.19524_19525insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000650711.1:c.343+203_343+204insA MANE Select ENSP00000498537.1:n.343+203_343+204insA
ENST00000261707.7:c.343+203_343+204insA ENSP00000261707.3:n.343+203_343+204insA
ENST00000394821.2:c.343+203_343+204insA ENSP00000378298.2:n.343+203_343+204insA
ENST00000401766.6:c.343+203_343+204insA ENSP00000385822.2:n.343+203_343+204insA
NM_001045.5:c.343+203_343+204insA NP_001036.1:n.343+203_343+204insA
NM_001045.6:c.343+203_343+204insA MANE Select NP_001036.1:n.343+203_343+204insA
Search 100 bp 5'
Search 100 bp 3'