Canonical Allele Identifier: CA1956619732

Gene: SLC6A5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.20627991T= , CM000673.2:g.20627991T=	GRCh38
NC_000011.9:g.20649537T= , CM000673.1:g.20649537T=	GRCh37
NC_000011.8:g.20606113T=	NCBI36
NG_013086.1:g.33592T=
NG_013086.2:g.33592T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525748.6:c.1407T= MANE Select	ENSP00000434364.2:p.Asp469=
ENST00000298923.11:c.*704T=	ENSP00000298923.7:n.*704T=
ENST00000525748.5:c.1407T=	ENSP00000434364.1:p.Asp469=
NM_004211.3:c.1407T=	NP_004202.2:p.Asp469=
XM_005253225.1:c.705T=	XP_005253282.1:p.Asp235=
XM_011520473.1:c.1407T=	XP_011518775.1:p.Asp469=
NM_001318369.1:c.705T=	NP_001305298.1:p.Asp235=
NM_004211.4:c.1407T=	NP_004202.3:p.Asp469=
XM_017018544.2:c.531T=	XP_016874033.1:p.Asp177=
XM_017018545.2:c.366T=	XP_016874034.1:p.Asp122=
NM_001318369.2:c.705T=	NP_001305298.1:p.Asp235=
NM_004211.5:c.1407T= MANE Select	NP_004202.4:p.Asp469=