Canonical Allele Identifier: CA2636978340
Gene: SLC6A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30221576_30221577insTCCGGTTCACAGCCCAC , CM000679.2:g.30221576_30221577insTCCGGTTCACAGCCCAC GRCh38
NC_000017.10:g.28548594_28548595insTCCGGTTCACAGCCCAC , CM000679.1:g.28548594_28548595insTCCGGTTCACAGCCCAC GRCh37
NC_000017.9:g.25572720_25572721insTCCGGTTCACAGCCCAC NCBI36
NG_011747.2:g.19371_19372insACCGGAGTGGGCTGTGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000650711.1:c.343+50_343+51insACCGGAGTGGGCTGTGA MANE Select ENSP00000498537.1:n.343+50_343+51insACCGGAGTGGGCTGTGA
ENST00000261707.7:c.343+50_343+51insACCGGAGTGGGCTGTGA ENSP00000261707.3:n.343+50_343+51insACCGGAGTGGGCTGTGA
ENST00000394821.2:c.343+50_343+51insACCGGAGTGGGCTGTGA ENSP00000378298.2:n.343+50_343+51insACCGGAGTGGGCTGTGA
ENST00000401766.6:c.343+50_343+51insACCGGAGTGGGCTGTGA ENSP00000385822.2:n.343+50_343+51insACCGGAGTGGGCTGTGA
NM_001045.5:c.343+50_343+51insACCGGAGTGGGCTGTGA NP_001036.1:n.343+50_343+51insACCGGAGTGGGCTGTGA
NM_001045.6:c.343+50_343+51insACCGGAGTGGGCTGTGA MANE Select NP_001036.1:n.343+50_343+51insACCGGAGTGGGCTGTGA