Canonical Allele Identifier: CA379917290

Gene: SLC6A5

Linked Data

• MyVariant Identifiers: chr11:g.20649586A>T (hg19) ; chr11:g.20628040A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.20628040A>T , CM000673.2:g.20628040A>T	GRCh38
NC_000011.9:g.20649586A>T , CM000673.1:g.20649586A>T	GRCh37
NC_000011.8:g.20606162A>T	NCBI36
NG_013086.1:g.33641A>T
NG_013086.2:g.33641A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525748.6:c.1456A>T MANE Select	ENSP00000434364.2:p.Ile486Phe
ENST00000298923.11:c.*753A>T	ENSP00000298923.7:n.*753A>T
ENST00000525748.5:c.1456A>T	ENSP00000434364.1:p.Ile486Phe
NM_004211.3:c.1456A>T	NP_004202.2:p.Ile486Phe
XM_005253225.1:c.754A>T	XP_005253282.1:p.Ile252Phe
XM_011520473.1:c.1456A>T	XP_011518775.1:p.Ile486Phe
NM_001318369.1:c.754A>T	NP_001305298.1:p.Ile252Phe
NM_004211.4:c.1456A>T	NP_004202.3:p.Ile486Phe
XM_017018544.2:c.580A>T	XP_016874033.1:p.Ile194Phe
XM_017018545.2:c.415A>T	XP_016874034.1:p.Ile139Phe
NM_001318369.2:c.754A>T	NP_001305298.1:p.Ile252Phe
NM_004211.5:c.1456A>T MANE Select	NP_004202.4:p.Ile486Phe