Canonical Allele Identifier: CA2255094079
Gene: SLC6A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30221562_30221579delinsCGGGTCACAGCCCACCCT , CM000679.2:g.30221562_30221579delinsCGGGTCACAGCCCACCCT GRCh38
NC_000017.10:g.28548580_28548597delinsCGGGTCACAGCCCACCCT , CM000679.1:g.28548580_28548597delinsCGGGTCACAGCCCACCCT GRCh37
NC_000017.9:g.25572706_25572723delinsCGGGTCACAGCCCACCCT NCBI36
NG_011747.2:g.19358_19375delinsAGGGTGGGCTGTGACCCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000650711.1:c.343+37_343+54delinsAGGGTGGGCTGTGACCCG MANE Select ENSP00000498537.1:n.343+37_343+54delinsAGGGTGGGCTGTGACCCG
ENST00000261707.7:c.343+37_343+54delinsAGGGTGGGCTGTGACCCG ENSP00000261707.3:n.343+37_343+54delinsAGGGTGGGCTGTGACCCG
ENST00000394821.2:c.343+37_343+54delinsAGGGTGGGCTGTGACCCG ENSP00000378298.2:n.343+37_343+54delinsAGGGTGGGCTGTGACCCG
ENST00000401766.6:c.343+37_343+54delinsAGGGTGGGCTGTGACCCG ENSP00000385822.2:n.343+37_343+54delinsAGGGTGGGCTGTGACCCG
NM_001045.5:c.343+37_343+54delinsAGGGTGGGCTGTGACCCG NP_001036.1:n.343+37_343+54delinsAGGGTGGGCTGTGACCCG
NM_001045.6:c.343+37_343+54delinsAGGGTGGGCTGTGACCCG MANE Select NP_001036.1:n.343+37_343+54delinsAGGGTGGGCTGTGACCCG