Canonical Allele Identifier: CA1590838568

Gene: SLC6A7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150201807G= , CM000667.2:g.150201807G=	GRCh38
NC_000005.9:g.149581370G= , CM000667.1:g.149581370G=	GRCh37
NC_000005.8:g.149561563G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000230671.7:c.859-540G= MANE Select	ENSP00000230671.2:n.859-540G=
ENST00000230671.6:c.859-540G=	ENSP00000230671.2:n.859-540G=
ENST00000524041.1:c.859-540G=	ENSP00000428200.1:n.859-540G=
NM_014228.3:c.859-540G=	NP_055043.2:n.859-540G=
NM_014228.4:c.859-540G=	NP_055043.2:n.859-540G=
XM_017009767.1:c.1213-540G=	XP_016865256.1:n.1213-540G=
XM_017009768.2:c.727-540G=	XP_016865257.1:n.727-540G=
XM_017009769.2:c.727-540G=	XP_016865258.1:n.727-540G=
XM_017009770.2:c.616-540G=	XP_016865259.1:n.616-540G=
XM_024446190.1:c.727-540G=	XP_024301958.1:n.727-540G=
XR_001742210.1:n.1233-540G=
XR_001742211.1:n.1233-540G=
XR_001742212.1:n.1122-540G=
NM_014228.5:c.859-540G= MANE Select	NP_055043.2:n.859-540G=