Canonical Allele Identifier: CA473404829

Gene: SLC6A5

Linked Data

• gnomAD v4: 11-20638461-T-C
• MyVariant Identifiers: chr11:g.20660007T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.20638461T>C , CM000673.2:g.20638461T>C	GRCh38
NC_000011.9:g.20660007T>C , CM000673.1:g.20660007T>C	GRCh37
NC_000011.8:g.20616583T>C	NCBI36
NG_013086.1:g.44062T>C
NG_013086.2:g.44062T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525748.6:c.1872T>C MANE Select	ENSP00000434364.2:p.Gly624=
ENST00000298923.11:c.*1169T>C	ENSP00000298923.7:n.*1169T>C
ENST00000525748.5:c.1872T>C	ENSP00000434364.1:p.Gly624=
ENST00000528440.1:n.403T>C
NM_004211.3:c.1872T>C	NP_004202.2:p.Gly624=
XM_005253225.1:c.1170T>C	XP_005253282.1:p.Gly390=
XM_011520473.1:c.1872T>C	XP_011518775.1:p.Gly624=
NM_001318369.1:c.1170T>C	NP_001305298.1:p.Gly390=
NM_004211.4:c.1872T>C	NP_004202.3:p.Gly624=
XM_017018544.2:c.996T>C	XP_016874033.1:p.Gly332=
XM_017018545.2:c.831T>C	XP_016874034.1:p.Gly277=
NM_001318369.2:c.1170T>C	NP_001305298.1:p.Gly390=
NM_004211.5:c.1872T>C MANE Select	NP_004202.4:p.Gly624=