Canonical Allele Identifier: CA379918594

Gene: SLC6A5

Linked Data

• MyVariant Identifiers: chr11:g.20660021T>A (hg19) ; chr11:g.20638475T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.20638475T>A , CM000673.2:g.20638475T>A	GRCh38
NC_000011.9:g.20660021T>A , CM000673.1:g.20660021T>A	GRCh37
NC_000011.8:g.20616597T>A	NCBI36
NG_013086.1:g.44076T>A
NG_013086.2:g.44076T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525748.6:c.1886T>A MANE Select	ENSP00000434364.2:p.Phe629Tyr
ENST00000298923.11:c.*1183T>A	ENSP00000298923.7:n.*1183T>A
ENST00000525748.5:c.1886T>A	ENSP00000434364.1:p.Phe629Tyr
ENST00000528440.1:n.417T>A
NM_004211.3:c.1886T>A	NP_004202.2:p.Phe629Tyr
XM_005253225.1:c.1184T>A	XP_005253282.1:p.Phe395Tyr
XM_011520473.1:c.1886T>A	XP_011518775.1:p.Phe629Tyr
NM_001318369.1:c.1184T>A	NP_001305298.1:p.Phe395Tyr
NM_004211.4:c.1886T>A	NP_004202.3:p.Phe629Tyr
XM_017018544.2:c.1010T>A	XP_016874033.1:p.Phe337Tyr
XM_017018545.2:c.845T>A	XP_016874034.1:p.Phe282Tyr
NM_001318369.2:c.1184T>A	NP_001305298.1:p.Phe395Tyr
NM_004211.5:c.1886T>A MANE Select	NP_004202.4:p.Phe629Tyr