Canonical Allele Identifier: CA391612699
Gene: SLC12A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2094419
ClinVar RCV Id: RCV003010279
MyVariant Identifiers: chr15:g.34549904C>T (hg19) chr15:g.34257703C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.34257703C>T , CM000677.2:g.34257703C>T GRCh38
NC_000015.9:g.34549904C>T , CM000677.1:g.34549904C>T GRCh37
NC_000015.8:g.32337196C>T NCBI36
NG_007951.1:g.85362G>A , LRG_270:g.85362G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000354181.8:c.629G>A MANE Select ENSP00000346112.3:p.Trp210Ter
ENST00000675289.1:n.1411G>A
ENST00000676379.1:c.629G>A ENSP00000502539.1:p.Trp210Ter
ENST00000290209.9:c.476G>A ENSP00000290209.5:p.Trp159Ter
ENST00000354181.7:c.629G>A ENSP00000346112.3:p.Trp210Ter
ENST00000397702.6:c.452G>A ENSP00000380814.2:p.Trp151Ter
ENST00000397707.6:c.584G>A ENSP00000380819.2:p.Trp195Ter
ENST00000458406.6:c.452G>A ENSP00000387725.2:p.Trp151Ter
ENST00000558589.5:c.602G>A ENSP00000452776.1:p.Trp201Ter
ENST00000558667.5:c.629G>A ENSP00000453473.1:p.Trp210Ter
ENST00000559523.5:c.452G>A ENSP00000452904.1:p.Trp151Ter
ENST00000559664.5:c.629G>A ENSP00000453702.1:p.Trp210Ter
ENST00000560164.5:c.126+1110G>A ENSP00000452705.1:n.126+1110G>A
ENST00000560332.1:c.212G>A ENSP00000454037.1:p.Trp71Ter
ENST00000560611.5:c.629G>A ENSP00000454168.1:p.Trp210Ter
ENST00000561080.5:c.629G>A ENSP00000454069.1:p.Trp210Ter
NM_001042494.1:c.452G>A NP_001035959.1:p.Trp151Ter
NM_001042495.1:c.452G>A NP_001035960.1:p.Trp151Ter
NM_001042496.1:c.602G>A NP_001035961.1:p.Trp201Ter
NM_001042497.1:c.584G>A NP_001035962.1:p.Trp195Ter
NM_005135.2:c.476G>A , LRG_270t1:c.476G>A NP_005126.1:p.Trp159Ter
NM_133647.1:c.629G>A , LRG_270t2:c.629G>A NP_598408.1:p.Trp210Ter
XM_006720793.2:c.543+1110G>A XP_006720856.1:n.543+1110G>A
XM_011522267.1:c.629G>A XP_011520569.1:p.Trp210Ter
XM_011522268.1:c.629G>A XP_011520570.1:p.Trp210Ter
XM_011522269.1:c.629G>A XP_011520571.1:p.Trp210Ter
XR_429476.2:n.635G>A
XR_931960.1:n.635G>A
XR_931961.1:n.635G>A
NM_001365088.1:c.629G>A MANE Select NP_001352017.1:p.Trp210Ter
XM_006720793.4:c.543+1110G>A XP_006720856.1:n.543+1110G>A
XM_011522269.3:c.629G>A XP_011520571.1:p.Trp210Ter
XR_931960.3:n.1879G>A
NM_001042494.2:c.452G>A NP_001035959.1:p.Trp151Ter
NM_001042495.2:c.452G>A NP_001035960.1:p.Trp151Ter
NM_001042496.2:c.602G>A NP_001035961.1:p.Trp201Ter
NM_001042497.2:c.584G>A NP_001035962.1:p.Trp195Ter
NM_133647.2:c.629G>A NP_598408.1:p.Trp210Ter
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