Canonical Allele Identifier: CA2255095578

Gene: SLC6A4

Linked Data

• dbSNP Id: rs1906888006

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30225070_30225071insG , CM000679.2:g.30225070_30225071insG	GRCh38
NC_000017.10:g.28552088_28552089insG , CM000679.1:g.28552088_28552089insG	GRCh37
NC_000017.9:g.25576214_25576215insG	NCBI36
NG_011747.2:g.15866_15867insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650711.1:c.-220-2156_-220-2155insC MANE Select	ENSP00000498537.1:n.-220-2156_-220-2155insC
ENST00000261707.7:c.-220-2156_-220-2155insC	ENSP00000261707.3:n.-220-2156_-220-2155insC
ENST00000394821.2:c.-220-2156_-220-2155insC	ENSP00000378298.2:n.-220-2156_-220-2155insC
ENST00000401766.6:c.-123-2990_-123-2989insC	ENSP00000385822.2:n.-123-2990_-123-2989insC
NM_001045.5:c.-220-2156_-220-2155insC	NP_001036.1:n.-220-2156_-220-2155insC
NM_001045.6:c.-220-2156_-220-2155insC MANE Select	NP_001036.1:n.-220-2156_-220-2155insC