Canonical Allele Identifier: CA379917360

Gene: SLC6A5

Linked Data

• MyVariant Identifiers: chr11:g.20649617A>C (hg19) ; chr11:g.20628071A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.20628071A>C , CM000673.2:g.20628071A>C	GRCh38
NC_000011.9:g.20649617A>C , CM000673.1:g.20649617A>C	GRCh37
NC_000011.8:g.20606193A>C	NCBI36
NG_013086.1:g.33672A>C
NG_013086.2:g.33672A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525748.6:c.1487A>C MANE Select	ENSP00000434364.2:p.Asn496Thr
ENST00000298923.11:c.*784A>C	ENSP00000298923.7:n.*784A>C
ENST00000525748.5:c.1487A>C	ENSP00000434364.1:p.Asn496Thr
NM_004211.3:c.1487A>C	NP_004202.2:p.Asn496Thr
XM_005253225.1:c.785A>C	XP_005253282.1:p.Asn262Thr
XM_011520473.1:c.1487A>C	XP_011518775.1:p.Asn496Thr
NM_001318369.1:c.785A>C	NP_001305298.1:p.Asn262Thr
NM_004211.4:c.1487A>C	NP_004202.3:p.Asn496Thr
XM_017018544.2:c.611A>C	XP_016874033.1:p.Asn204Thr
XM_017018545.2:c.446A>C	XP_016874034.1:p.Asn149Thr
NM_001318369.2:c.785A>C	NP_001305298.1:p.Asn262Thr
NM_004211.5:c.1487A>C MANE Select	NP_004202.4:p.Asn496Thr