Canonical Allele Identifier: CA919823701
Gene: SLC6A4 HGNC NCBI

Linked Data

dbSNP Id: rs1597637121
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30211443_30211444insAATG , CM000679.2:g.30211443_30211444insAATG GRCh38
NC_000017.10:g.28538461_28538462insAATG , CM000679.1:g.28538461_28538462insAATG GRCh37
NC_000017.9:g.25562587_25562588insAATG NCBI36
NG_011747.2:g.29493_29494insCATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000650711.1:c.1205-20_1205-19insCATT MANE Select ENSP00000498537.1:n.1205-20_1205-19insCATT
ENST00000261707.7:c.1205-20_1205-19insCATT ENSP00000261707.3:n.1205-20_1205-19insCATT
ENST00000394821.2:c.1205-20_1205-19insCATT ENSP00000378298.2:n.1205-20_1205-19insCATT
ENST00000401766.6:c.1205-20_1205-19insCATT ENSP00000385822.2:n.1205-20_1205-19insCATT
NM_001045.5:c.1205-20_1205-19insCATT NP_001036.1:n.1205-20_1205-19insCATT
NM_001045.6:c.1205-20_1205-19insCATT MANE Select NP_001036.1:n.1205-20_1205-19insCATT
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