Canonical Allele Identifier: CA14486446

Gene: SLC6A4

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30204775C>T , CM000679.2:g.30204775C>T	GRCh38
NC_000017.10:g.28531793C>T , CM000679.1:g.28531793C>T	GRCh37
NC_000017.9:g.25555919C>T	NCBI36
NG_011747.2:g.36162G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650711.1:c.1651-1436G>A MANE Select	ENSP00000498537.1:n.1651-1436G>A
ENST00000261707.7:c.1651-1436G>A	ENSP00000261707.3:n.1651-1436G>A
ENST00000394821.2:c.1651-1436G>A	ENSP00000378298.2:n.1651-1436G>A
ENST00000401766.6:c.1651-1436G>A	ENSP00000385822.2:n.1651-1436G>A
ENST00000579221.5:c.292-1436G>A
NM_001045.5:c.1651-1436G>A	NP_001036.1:n.1651-1436G>A
NM_001045.6:c.1651-1436G>A MANE Select	NP_001036.1:n.1651-1436G>A