Canonical Allele Identifier: CA391612748

Gene: SLC12A6

Linked Data

• ClinVar Variation Id: 521402
• ClinVar RCV Id: RCV000623060 ; RCV002287895 ; RCV002532836
• dbSNP Id: rs1555381416
• MyVariant Identifiers: chr15:g.34549913C>T (hg19) ; chr15:g.34257712C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.34257712C>T , CM000677.2:g.34257712C>T	GRCh38
NC_000015.9:g.34549913C>T , CM000677.1:g.34549913C>T	GRCh37
NC_000015.8:g.32337205C>T	NCBI36
NG_007951.1:g.85353G>A , LRG_270:g.85353G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354181.8:c.620G>A MANE Select	ENSP00000346112.3:p.Arg207His
ENST00000675289.1:n.1402G>A
ENST00000676379.1:c.620G>A	ENSP00000502539.1:p.Arg207His
ENST00000290209.9:c.467G>A	ENSP00000290209.5:p.Arg156His
ENST00000354181.7:c.620G>A	ENSP00000346112.3:p.Arg207His
ENST00000397702.6:c.443G>A	ENSP00000380814.2:p.Arg148His
ENST00000397707.6:c.575G>A	ENSP00000380819.2:p.Arg192His
ENST00000458406.6:c.443G>A	ENSP00000387725.2:p.Arg148His
ENST00000558589.5:c.593G>A	ENSP00000452776.1:p.Arg198His
ENST00000558667.5:c.620G>A	ENSP00000453473.1:p.Arg207His
ENST00000559523.5:c.443G>A	ENSP00000452904.1:p.Arg148His
ENST00000559664.5:c.620G>A	ENSP00000453702.1:p.Arg207His
ENST00000560164.5:c.126+1101G>A	ENSP00000452705.1:n.126+1101G>A
ENST00000560332.1:c.203G>A	ENSP00000454037.1:p.Arg68His
ENST00000560611.5:c.620G>A	ENSP00000454168.1:p.Arg207His
ENST00000561080.5:c.620G>A	ENSP00000454069.1:p.Arg207His
NM_001042494.1:c.443G>A	NP_001035959.1:p.Arg148His
NM_001042495.1:c.443G>A	NP_001035960.1:p.Arg148His
NM_001042496.1:c.593G>A	NP_001035961.1:p.Arg198His
NM_001042497.1:c.575G>A	NP_001035962.1:p.Arg192His
NM_005135.2:c.467G>A , LRG_270t1:c.467G>A	NP_005126.1:p.Arg156His
NM_133647.1:c.620G>A , LRG_270t2:c.620G>A	NP_598408.1:p.Arg207His
XM_006720793.2:c.543+1101G>A	XP_006720856.1:n.543+1101G>A
XM_011522267.1:c.620G>A	XP_011520569.1:p.Arg207His
XM_011522268.1:c.620G>A	XP_011520570.1:p.Arg207His
XM_011522269.1:c.620G>A	XP_011520571.1:p.Arg207His
XR_429476.2:n.626G>A
XR_931960.1:n.626G>A
XR_931961.1:n.626G>A
NM_001365088.1:c.620G>A MANE Select	NP_001352017.1:p.Arg207His
XM_006720793.4:c.543+1101G>A	XP_006720856.1:n.543+1101G>A
XM_011522269.3:c.620G>A	XP_011520571.1:p.Arg207His
XR_931960.3:n.1870G>A
NM_001042494.2:c.443G>A	NP_001035959.1:p.Arg148His
NM_001042495.2:c.443G>A	NP_001035960.1:p.Arg148His
NM_001042496.2:c.593G>A	NP_001035961.1:p.Arg198His
NM_001042497.2:c.575G>A	NP_001035962.1:p.Arg192His
NM_133647.2:c.620G>A	NP_598408.1:p.Arg207His