Canonical Allele Identifier: CA398960597

Gene: SLC6A4

Linked Data

• MyVariant Identifiers: chr17:g.28548656G>T (hg19) ; chr17:g.30221638G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30221638G>T , CM000679.2:g.30221638G>T	GRCh38
NC_000017.10:g.28548656G>T , CM000679.1:g.28548656G>T	GRCh37
NC_000017.9:g.25572782G>T	NCBI36
NG_011747.2:g.19299C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650711.1:c.321C>A MANE Select	ENSP00000498537.1:p.Tyr107Ter
ENST00000261707.7:c.321C>A	ENSP00000261707.3:p.Tyr107Ter
ENST00000394821.2:c.321C>A	ENSP00000378298.2:p.Tyr107Ter
ENST00000401766.6:c.321C>A	ENSP00000385822.2:p.Tyr107Ter
NM_001045.5:c.321C>A	NP_001036.1:p.Tyr107Ter
NM_001045.6:c.321C>A MANE Select	NP_001036.1:p.Tyr107Ter