Canonical Allele Identifier: CA1590838546

Gene: SLC6A7

Linked Data

• dbSNP Id: rs1753395508

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150201760A>G , CM000667.2:g.150201760A>G	GRCh38
NC_000005.9:g.149581323A>G , CM000667.1:g.149581323A>G	GRCh37
NC_000005.8:g.149561516A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000230671.7:c.858+537A>G MANE Select	ENSP00000230671.2:n.858+537A>G
ENST00000230671.6:c.858+537A>G	ENSP00000230671.2:n.858+537A>G
ENST00000524041.1:c.858+537A>G	ENSP00000428200.1:n.858+537A>G
NM_014228.3:c.858+537A>G	NP_055043.2:n.858+537A>G
NM_014228.4:c.858+537A>G	NP_055043.2:n.858+537A>G
XM_017009767.1:c.1212+537A>G	XP_016865256.1:n.1212+537A>G
XM_017009768.2:c.726+537A>G	XP_016865257.1:n.726+537A>G
XM_017009769.2:c.726+537A>G	XP_016865258.1:n.726+537A>G
XM_017009770.2:c.615+537A>G	XP_016865259.1:n.615+537A>G
XM_024446190.1:c.726+537A>G	XP_024301958.1:n.726+537A>G
XR_001742210.1:n.1232+537A>G
XR_001742211.1:n.1232+537A>G
XR_001742212.1:n.1121+537A>G
NM_014228.5:c.858+537A>G MANE Select	NP_055043.2:n.858+537A>G