Canonical Allele Identifier: CA379917193

Gene: SLC6A5

Linked Data

• dbSNP Id: rs1853033267
• gnomAD v4: 11-20627995-G-A
• MyVariant Identifiers: chr11:g.20649541G>A (hg19) ; chr11:g.20627995G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.20627995G>A , CM000673.2:g.20627995G>A	GRCh38
NC_000011.9:g.20649541G>A , CM000673.1:g.20649541G>A	GRCh37
NC_000011.8:g.20606117G>A	NCBI36
NG_013086.1:g.33596G>A
NG_013086.2:g.33596G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525748.6:c.1411G>A MANE Select	ENSP00000434364.2:p.Ala471Thr
ENST00000298923.11:c.*708G>A	ENSP00000298923.7:n.*708G>A
ENST00000525748.5:c.1411G>A	ENSP00000434364.1:p.Ala471Thr
NM_004211.3:c.1411G>A	NP_004202.2:p.Ala471Thr
XM_005253225.1:c.709G>A	XP_005253282.1:p.Ala237Thr
XM_011520473.1:c.1411G>A	XP_011518775.1:p.Ala471Thr
NM_001318369.1:c.709G>A	NP_001305298.1:p.Ala237Thr
NM_004211.4:c.1411G>A	NP_004202.3:p.Ala471Thr
XM_017018544.2:c.535G>A	XP_016874033.1:p.Ala179Thr
XM_017018545.2:c.370G>A	XP_016874034.1:p.Ala124Thr
NM_001318369.2:c.709G>A	NP_001305298.1:p.Ala237Thr
NM_004211.5:c.1411G>A MANE Select	NP_004202.4:p.Ala471Thr