Canonical Allele Identifier: CA597487745

Gene: SLC6A5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.20638562A>T , CM000673.2:g.20638562A>T	GRCh38
NC_000011.9:g.20660108A>T , CM000673.1:g.20660108A>T	GRCh37
NC_000011.8:g.20616684A>T	NCBI36
NG_013086.1:g.44163A>T
NG_013086.2:g.44163A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004211.5:c.1969+4A>T MANE Select	NP_004202.4:n.1969+4A>T
ENST00000525748.6:c.1969+4A>T MANE Select	ENSP00000434364.2:n.1969+4A>T
NM_001318369.1:c.1267+4A>T	NP_001305298.1:n.1267+4A>T
NM_001318369.2:c.1267+4A>T	NP_001305298.1:n.1267+4A>T
NM_004211.3:c.1969+4A>T	NP_004202.2:n.1969+4A>T
NM_004211.4:c.1969+4A>T	NP_004202.3:n.1969+4A>T
ENST00000298923.11:c.*1266+4A>T	ENSP00000298923.7:n.*1266+4A>T
ENST00000525748.5:c.1969+4A>T	ENSP00000434364.1:n.1969+4A>T
ENST00000528440.1:n.500+4A>T
XM_005253225.1:c.1267+4A>T	XP_005253282.1:n.1267+4A>T
XM_011520473.1:c.1969+4A>T	XP_011518775.1:n.1969+4A>T
XM_017018544.2:c.1093+4A>T	XP_016874033.1:n.1093+4A>T
XM_017018545.2:c.928+4A>T	XP_016874034.1:n.928+4A>T