Canonical Allele Identifier: CA391621320
Community Standard Title: NM_001365088.1(SLC12A6):c.1655G>A (p.Gly552Asp)
Gene: SLC12A6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.34245862C>T , CM000677.2:g.34245862C>T GRCh38
NC_000015.9:g.34538063C>T , CM000677.1:g.34538063C>T GRCh37
NC_000015.8:g.32325355C>T NCBI36
NG_007951.1:g.97203G>A , LRG_270:g.97203G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001365088.1:c.1655G>A MANE Select NP_001352017.1:p.Gly552Asp
ENST00000354181.8:c.1655G>A MANE Select ENSP00000346112.3:p.Gly552Asp
NM_001042494.1:c.1478G>A NP_001035959.1:p.Gly493Asp
NM_001042494.2:c.1478G>A NP_001035959.1:p.Gly493Asp
NM_001042495.1:c.1478G>A NP_001035960.1:p.Gly493Asp
NM_001042495.2:c.1478G>A NP_001035960.1:p.Gly493Asp
NM_001042496.1:c.1628G>A NP_001035961.1:p.Gly543Asp
NM_001042496.2:c.1628G>A NP_001035961.1:p.Gly543Asp
NM_001042497.1:c.1610G>A NP_001035962.1:p.Gly537Asp
NM_001042497.2:c.1610G>A NP_001035962.1:p.Gly537Asp
NM_005135.2:c.1502G>A , LRG_270t1:c.1502G>A NP_005126.1:p.Gly501Asp
NM_133647.1:c.1655G>A , LRG_270t2:c.1655G>A NP_598408.1:p.Gly552Asp
NM_133647.2:c.1655G>A NP_598408.1:p.Gly552Asp
ENST00000290209.9:c.1502G>A ENSP00000290209.5:p.Gly501Asp
ENST00000354181.7:c.1655G>A ENSP00000346112.3:p.Gly552Asp
ENST00000397702.6:c.1478G>A ENSP00000380814.2:p.Gly493Asp
ENST00000397707.6:c.1610G>A ENSP00000380819.2:p.Gly537Asp
ENST00000458406.6:c.1478G>A ENSP00000387725.2:p.Gly493Asp
ENST00000558589.5:c.1628G>A ENSP00000452776.1:p.Gly543Asp
ENST00000558667.5:c.1655G>A ENSP00000453473.1:p.Gly552Asp
ENST00000559523.5:c.1478G>A ENSP00000452904.1:p.Gly493Asp
ENST00000559664.5:c.1655G>A ENSP00000453702.1:p.Gly552Asp
ENST00000560164.5:c.1091G>A ENSP00000452705.1:p.Gly364Asp
ENST00000560611.5:c.1655G>A ENSP00000454168.1:p.Gly552Asp
ENST00000561080.5:c.1655G>A ENSP00000454069.1:p.Gly552Asp
ENST00000675289.1:n.2437G>A
ENST00000676379.1:c.1655G>A ENSP00000502539.1:p.Gly552Asp
XM_006720793.2:c.1508G>A XP_006720856.1:p.Gly503Asp
XM_006720793.4:c.1508G>A XP_006720856.1:p.Gly503Asp
XM_011522267.1:c.1655G>A XP_011520569.1:p.Gly552Asp
XM_011522268.1:c.1655G>A XP_011520570.1:p.Gly552Asp
XM_011522269.1:c.1655G>A XP_011520571.1:p.Gly552Asp
XM_011522269.3:c.1655G>A XP_011520571.1:p.Gly552Asp
XR_429476.2:n.1661G>A
XR_931960.1:n.1661G>A
XR_931960.3:n.2905G>A
XR_931961.1:n.1661G>A