Canonical Allele Identifier: CA218727342

Gene: SLC6A5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.20617515C>T , CM000673.2:g.20617515C>T	GRCh38
NC_000011.9:g.20639061C>T , CM000673.1:g.20639061C>T	GRCh37
NC_000011.8:g.20595637C>T	NCBI36
NG_013086.1:g.23116C>T
NG_013086.2:g.23116C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525748.6:c.1128-237C>T MANE Select	ENSP00000434364.2:n.1128-237C>T
ENST00000298923.11:c.*425-237C>T	ENSP00000298923.7:n.*425-237C>T
ENST00000525748.5:c.1128-237C>T	ENSP00000434364.1:n.1128-237C>T
NM_004211.3:c.1128-237C>T	NP_004202.2:n.1128-237C>T
XM_005253225.1:c.426-237C>T	XP_005253282.1:n.426-237C>T
XM_011520473.1:c.1128-237C>T	XP_011518775.1:n.1128-237C>T
NM_001318369.1:c.426-237C>T	NP_001305298.1:n.426-237C>T
NM_004211.4:c.1128-237C>T	NP_004202.3:n.1128-237C>T
XM_017018544.2:c.252-237C>T	XP_016874033.1:n.252-237C>T
XM_017018545.2:c.87-237C>T	XP_016874034.1:n.87-237C>T
NM_001318369.2:c.426-237C>T	NP_001305298.1:n.426-237C>T
NM_004211.5:c.1128-237C>T MANE Select	NP_004202.4:n.1128-237C>T