Canonical Allele Identifier: CA499053313
Gene: SLC47A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.19611776C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.19708463C>G , CM000679.2:g.19708463C>G GRCh38
NC_000017.10:g.19611776C>G , CM000679.1:g.19611776C>G GRCh37
NC_000017.9:g.19552368C>G NCBI36
NG_052805.1:g.15517G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000433844.4:c.532-64G>C MANE Select ENSP00000391848.3:n.532-64G>C
ENST00000325411.9:c.576G>C ENSP00000326671.5:p.Pro192=
ENST00000350657.9:c.532-64G>C ENSP00000338084.6:n.532-64G>C
ENST00000433844.2:c.532-64G>C ENSP00000391848.2:n.532-64G>C
ENST00000463318.5:n.1278-64G>C
ENST00000467379.1:n.1672G>C
ENST00000467609.5:n.543-64G>C
ENST00000574220.5:n.396-39G>C
ENST00000574239.5:c.622G>C ENSP00000458694.1:p.Gly208Arg
NM_001099646.1:c.532-64G>C NP_001093116.1:n.532-64G>C
NM_001256663.1:c.532-64G>C NP_001243592.1:n.532-64G>C
NM_152908.3:c.576G>C NP_690872.2:p.Pro192=
XM_006721455.2:c.532-64G>C XP_006721518.1:n.532-64G>C
XM_006721457.2:c.532-64G>C XP_006721520.1:n.532-64G>C
XM_011523672.1:c.490-64G>C XP_011521974.1:n.490-64G>C
XM_011523673.1:c.385-64G>C XP_011521975.1:n.385-64G>C
XM_011523674.1:c.385-64G>C XP_011521976.1:n.385-64G>C
XM_011523675.1:c.532-64G>C XP_011521977.1:n.532-64G>C
XR_243543.3:n.1141-64G>C
XR_933998.1:n.641-64G>C
XR_933999.1:n.641-64G>C
XR_934000.1:n.641-64G>C
XR_934001.1:n.641-64G>C
NR_135624.1:n.1278-64G>C
NR_135625.1:n.797G>C
XM_017024221.1:c.576G>C XP_016879710.1:p.Pro192=
XM_017024222.2:c.429G>C XP_016879711.1:p.Pro143=
XM_017024223.1:c.576G>C XP_016879712.1:p.Pro192=
XM_017024224.1:c.576G>C XP_016879713.1:p.Pro192=
XM_017024225.1:c.576G>C XP_016879714.1:p.Pro192=
XM_017024226.1:c.576G>C XP_016879715.1:p.Pro192=
XR_001752432.1:n.685G>C
XR_001752433.1:n.685G>C
NM_001099646.2:c.532-64G>C NP_001093116.1:n.532-64G>C
NM_001256663.2:c.532-64G>C NP_001243592.1:n.532-64G>C
NM_152908.4:c.576G>C NP_690872.2:p.Pro192=
NR_135625.2:n.651G>C
NM_001099646.3:c.532-64G>C MANE Select NP_001093116.1:n.532-64G>C
NM_001256663.3:c.532-64G>C NP_001243592.1:n.532-64G>C
NM_152908.5:c.576G>C NP_690872.2:p.Pro192=
NR_135624.2:n.1278-64G>C
NR_135625.3:n.651G>C