Canonical Allele Identifier: CA1956624636

Gene: SLC6A5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.20638390G= , CM000673.2:g.20638390G=	GRCh38
NC_000011.9:g.20659936G= , CM000673.1:g.20659936G=	GRCh37
NC_000011.8:g.20616512G=	NCBI36
NG_013086.1:g.43991G=
NG_013086.2:g.43991G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000525748.6:c.1870-69G= MANE Select	ENSP00000434364.2:n.1870-69G=
ENST00000298923.11:c.*1167-69G=	ENSP00000298923.7:n.*1167-69G=
ENST00000525748.5:c.1870-69G=	ENSP00000434364.1:n.1870-69G=
ENST00000528440.1:n.401-69G=
NM_004211.3:c.1870-69G=	NP_004202.2:n.1870-69G=
XM_005253225.1:c.1168-69G=	XP_005253282.1:n.1168-69G=
XM_011520473.1:c.1870-69G=	XP_011518775.1:n.1870-69G=
NM_001318369.1:c.1168-69G=	NP_001305298.1:n.1168-69G=
NM_004211.4:c.1870-69G=	NP_004202.3:n.1870-69G=
XM_017018544.2:c.994-69G=	XP_016874033.1:n.994-69G=
XM_017018545.2:c.829-69G=	XP_016874034.1:n.829-69G=
NM_001318369.2:c.1168-69G=	NP_001305298.1:n.1168-69G=
NM_004211.5:c.1870-69G= MANE Select	NP_004202.4:n.1870-69G=