Canonical Allele Identifier: CA379918606

Gene: SLC6A5

Linked Data

• MyVariant Identifiers: chr11:g.20660026C>A (hg19) ; chr11:g.20638480C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.20638480C>A , CM000673.2:g.20638480C>A	GRCh38
NC_000011.9:g.20660026C>A , CM000673.1:g.20660026C>A	GRCh37
NC_000011.8:g.20616602C>A	NCBI36
NG_013086.1:g.44081C>A
NG_013086.2:g.44081C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525748.6:c.1891C>A MANE Select	ENSP00000434364.2:p.Leu631Ile
ENST00000298923.11:c.*1188C>A	ENSP00000298923.7:n.*1188C>A
ENST00000525748.5:c.1891C>A	ENSP00000434364.1:p.Leu631Ile
ENST00000528440.1:n.422C>A
NM_004211.3:c.1891C>A	NP_004202.2:p.Leu631Ile
XM_005253225.1:c.1189C>A	XP_005253282.1:p.Leu397Ile
XM_011520473.1:c.1891C>A	XP_011518775.1:p.Leu631Ile
NM_001318369.1:c.1189C>A	NP_001305298.1:p.Leu397Ile
NM_004211.4:c.1891C>A	NP_004202.3:p.Leu631Ile
XM_017018544.2:c.1015C>A	XP_016874033.1:p.Leu339Ile
XM_017018545.2:c.850C>A	XP_016874034.1:p.Leu284Ile
NM_001318369.2:c.1189C>A	NP_001305298.1:p.Leu397Ile
NM_004211.5:c.1891C>A MANE Select	NP_004202.4:p.Leu631Ile