Canonical Allele Identifier: CA379917291

Gene: SLC6A5

Linked Data

• MyVariant Identifiers: chr11:g.20649587T>A (hg19) ; chr11:g.20628041T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.20628041T>A , CM000673.2:g.20628041T>A	GRCh38
NC_000011.9:g.20649587T>A , CM000673.1:g.20649587T>A	GRCh37
NC_000011.8:g.20606163T>A	NCBI36
NG_013086.1:g.33642T>A
NG_013086.2:g.33642T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525748.6:c.1457T>A MANE Select	ENSP00000434364.2:p.Ile486Asn
ENST00000298923.11:c.*754T>A	ENSP00000298923.7:n.*754T>A
ENST00000525748.5:c.1457T>A	ENSP00000434364.1:p.Ile486Asn
NM_004211.3:c.1457T>A	NP_004202.2:p.Ile486Asn
XM_005253225.1:c.755T>A	XP_005253282.1:p.Ile252Asn
XM_011520473.1:c.1457T>A	XP_011518775.1:p.Ile486Asn
NM_001318369.1:c.755T>A	NP_001305298.1:p.Ile252Asn
NM_004211.4:c.1457T>A	NP_004202.3:p.Ile486Asn
XM_017018544.2:c.581T>A	XP_016874033.1:p.Ile194Asn
XM_017018545.2:c.416T>A	XP_016874034.1:p.Ile139Asn
NM_001318369.2:c.755T>A	NP_001305298.1:p.Ile252Asn
NM_004211.5:c.1457T>A MANE Select	NP_004202.4:p.Ile486Asn