Canonical Allele Identifier: CA14419484

Gene: SLC6A4

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30234442A>G , CM000679.2:g.30234442A>G	GRCh38
NC_000017.10:g.28561460A>G , CM000679.1:g.28561460A>G	GRCh37
NC_000017.9:g.25585586A>G	NCBI36
NG_011747.2:g.6495T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650711.1:c.-221+1171T>C MANE Select	ENSP00000498537.1:n.-221+1171T>C
ENST00000261707.7:c.-221+1171T>C	ENSP00000261707.3:n.-221+1171T>C
ENST00000394821.2:c.-221+1171T>C	ENSP00000378298.2:n.-221+1171T>C
ENST00000401766.6:c.-124+1171T>C	ENSP00000385822.2:n.-124+1171T>C
NM_001045.5:c.-221+1171T>C	NP_001036.1:n.-221+1171T>C
NM_001045.6:c.-221+1171T>C MANE Select	NP_001036.1:n.-221+1171T>C