Canonical Allele Identifier: CA1956619759

Gene: SLC6A5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.20628048_20628051delinsCTCT , CM000673.2:g.20628048_20628051delinsCTCT	GRCh38
NC_000011.9:g.20649594_20649597delinsCTCT , CM000673.1:g.20649594_20649597delinsCTCT	GRCh37
NC_000011.8:g.20606170_20606173delinsCTCT	NCBI36
NG_013086.1:g.33649_33652delinsCTCT
NG_013086.2:g.33649_33652delinsCTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525748.6:c.1464_1467delinsCTCT MANE Select	ENSP00000434364.2:p.Leu488=
ENST00000298923.11:c.*761_*764delinsCTCT	ENSP00000298923.7:n.*761_*764delinsCTCT
ENST00000525748.5:c.1464_1467delinsCTCT	ENSP00000434364.1:p.Leu488=
NM_004211.3:c.1464_1467delinsCTCT	NP_004202.2:p.Leu488=
XM_005253225.1:c.762_765delinsCTCT	XP_005253282.1:p.Leu254=
XM_011520473.1:c.1464_1467delinsCTCT	XP_011518775.1:p.Leu488=
NM_001318369.1:c.762_765delinsCTCT	NP_001305298.1:p.Leu254=
NM_004211.4:c.1464_1467delinsCTCT	NP_004202.3:p.Leu488=
XM_017018544.2:c.588_591delinsCTCT	XP_016874033.1:p.Leu196=
XM_017018545.2:c.423_426delinsCTCT	XP_016874034.1:p.Leu141=
NM_001318369.2:c.762_765delinsCTCT	NP_001305298.1:p.Leu254=
NM_004211.5:c.1464_1467delinsCTCT MANE Select	NP_004202.4:p.Leu488=