Canonical Allele Identifier: CA1590838572

Gene: SLC6A7

Linked Data

• dbSNP Id: rs1753397972

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150201818C>T , CM000667.2:g.150201818C>T	GRCh38
NC_000005.9:g.149581381C>T , CM000667.1:g.149581381C>T	GRCh37
NC_000005.8:g.149561574C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000230671.7:c.859-529C>T MANE Select	ENSP00000230671.2:n.859-529C>T
ENST00000230671.6:c.859-529C>T	ENSP00000230671.2:n.859-529C>T
ENST00000524041.1:c.859-529C>T	ENSP00000428200.1:n.859-529C>T
NM_014228.3:c.859-529C>T	NP_055043.2:n.859-529C>T
NM_014228.4:c.859-529C>T	NP_055043.2:n.859-529C>T
XM_017009767.1:c.1213-529C>T	XP_016865256.1:n.1213-529C>T
XM_017009768.2:c.727-529C>T	XP_016865257.1:n.727-529C>T
XM_017009769.2:c.727-529C>T	XP_016865258.1:n.727-529C>T
XM_017009770.2:c.616-529C>T	XP_016865259.1:n.616-529C>T
XM_024446190.1:c.727-529C>T	XP_024301958.1:n.727-529C>T
XR_001742210.1:n.1233-529C>T
XR_001742211.1:n.1233-529C>T
XR_001742212.1:n.1122-529C>T
NM_014228.5:c.859-529C>T MANE Select	NP_055043.2:n.859-529C>T