Canonical Allele Identifier: CA379918565

Gene: SLC6A5

Linked Data

• MyVariant Identifiers: chr11:g.20660008G>C (hg19) ; chr11:g.20638462G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.20638462G>C , CM000673.2:g.20638462G>C	GRCh38
NC_000011.9:g.20660008G>C , CM000673.1:g.20660008G>C	GRCh37
NC_000011.8:g.20616584G>C	NCBI36
NG_013086.1:g.44063G>C
NG_013086.2:g.44063G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525748.6:c.1873G>C MANE Select	ENSP00000434364.2:p.Gly625Arg
ENST00000298923.11:c.*1170G>C	ENSP00000298923.7:n.*1170G>C
ENST00000525748.5:c.1873G>C	ENSP00000434364.1:p.Gly625Arg
ENST00000528440.1:n.404G>C
NM_004211.3:c.1873G>C	NP_004202.2:p.Gly625Arg
XM_005253225.1:c.1171G>C	XP_005253282.1:p.Gly391Arg
XM_011520473.1:c.1873G>C	XP_011518775.1:p.Gly625Arg
NM_001318369.1:c.1171G>C	NP_001305298.1:p.Gly391Arg
NM_004211.4:c.1873G>C	NP_004202.3:p.Gly625Arg
XM_017018544.2:c.997G>C	XP_016874033.1:p.Gly333Arg
XM_017018545.2:c.832G>C	XP_016874034.1:p.Gly278Arg
NM_001318369.2:c.1171G>C	NP_001305298.1:p.Gly391Arg
NM_004211.5:c.1873G>C MANE Select	NP_004202.4:p.Gly625Arg