Canonical Allele Identifier: CA2255105464
Gene: SLC6A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30211793_30211797delinsCAGTT , CM000679.2:g.30211793_30211797delinsCAGTT GRCh38
NC_000017.10:g.28538811_28538815delinsCAGTT , CM000679.1:g.28538811_28538815delinsCAGTT GRCh37
NC_000017.9:g.25562937_25562941delinsCAGTT NCBI36
NG_011747.2:g.29140_29144delinsAACTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000650711.1:c.1205-373_1205-369delinsAACTG MANE Select ENSP00000498537.1:n.1205-373_1205-369delinsAACTG
ENST00000261707.7:c.1205-373_1205-369delinsAACTG ENSP00000261707.3:n.1205-373_1205-369delinsAACTG
ENST00000394821.2:c.1205-373_1205-369delinsAACTG ENSP00000378298.2:n.1205-373_1205-369delinsAACTG
ENST00000401766.6:c.1205-373_1205-369delinsAACTG ENSP00000385822.2:n.1205-373_1205-369delinsAACTG
NM_001045.5:c.1205-373_1205-369delinsAACTG NP_001036.1:n.1205-373_1205-369delinsAACTG
NM_001045.6:c.1205-373_1205-369delinsAACTG MANE Select NP_001036.1:n.1205-373_1205-369delinsAACTG