Canonical Allele Identifier: CA1991849878

Gene: SLC36A4

Linked Data

• dbSNP Id: rs12296063

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.93187236C>G , CM000673.2:g.93187236C>G	GRCh38
NC_000011.9:g.92920402C>G , CM000673.1:g.92920402C>G	GRCh37
NC_000011.8:g.92560050C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000326402.9:c.56-1422G>C MANE Select	ENSP00000317382.4:n.56-1422G>C
ENST00000326402.8:c.56-1422G>C	ENSP00000317382.4:n.56-1422G>C
ENST00000524875.1:c.56-1422G>C	ENSP00000434879.1:n.56-1422G>C
ENST00000527743.1:n.153-1422G>C
ENST00000529184.5:c.-321-1422G>C	ENSP00000436570.1:n.-321-1422G>C
NM_001286139.1:c.-321-1422G>C	NP_001273068.1:n.-321-1422G>C
NM_152313.3:c.56-1422G>C	NP_689526.2:n.56-1422G>C
XM_006718763.2:c.56-1422G>C	XP_006718826.1:n.56-1422G>C
XM_017017174.1:c.56-1422G>C	XP_016872663.1:n.56-1422G>C
XM_017017175.1:c.-172-1422G>C	XP_016872664.1:n.-172-1422G>C
XM_017017176.1:c.-230-1422G>C	XP_016872665.1:n.-230-1422G>C
XM_017017177.2:c.-321-1422G>C	XP_016872666.1:n.-321-1422G>C
XM_024448341.1:c.-2-1422G>C	XP_024304109.1:n.-2-1422G>C
XM_024448342.1:c.-321-1422G>C	XP_024304110.1:n.-321-1422G>C
XM_024448343.1:c.-601-1422G>C	XP_024304111.1:n.-601-1422G>C
XM_024448344.1:c.-572-1422G>C	XP_024304112.1:n.-572-1422G>C
XR_001747768.1:n.203-1422G>C
NM_152313.4:c.56-1422G>C MANE Select	NP_689526.2:n.56-1422G>C
NM_001286139.2:c.-321-1422G>C	NP_001273068.1:n.-321-1422G>C