Canonical Allele Identifier: CA10641562
Gene: SLC12A6 HGNC NCBI
EMC4 HGNC NCBI

Linked Data

ClinVar Variation Id: 315544
ClinVar RCV Id: RCV000399706
dbSNP Id: rs566558212

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.34230156dup , CM000677.2:g.34230156dup GRCh38
NC_000015.9:g.34522357dup , CM000677.1:g.34522357dup GRCh37
NC_000015.8:g.32309649dup NCBI36
NG_007951.1:g.112915dup , LRG_270:g.112915dup
NG_054746.1:g.10160dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000354181.8:c.*3731dup (SLC12A6) MANE Select ENSP00000346112.3:n.*3731dup
ENST00000676379.1:c.*2350dup (SLC12A6) ENSP00000502539.1:n.*2350dup
ENST00000290209.9:c.*3731dup (SLC12A6) ENSP00000290209.5:n.*3731dup
NM_001042494.1:c.*3731dup (SLC12A6) NP_001035959.1:n.*3731dup
NM_001042495.1:c.*3731dup (SLC12A6) NP_001035960.1:n.*3731dup
NM_001042496.1:c.*3731dup (SLC12A6) NP_001035961.1:n.*3731dup
NM_001042497.1:c.*3731dup (SLC12A6) NP_001035962.1:n.*3731dup
NM_001286420.1:c.*309dup (EMC4) NP_001273349.1:n.*309dup
NM_005135.2:c.*3731dup , LRG_270t1:c.*3731dup (SLC12A6) NP_005126.1:n.*3731dup
NM_016454.3:c.*368dup (EMC4) NP_057538.1:n.*368dup
NM_133647.1:c.*3731dup , LRG_270t2:c.*3731dup (SLC12A6) NP_598408.1:n.*3731dup
XM_011522267.1:c.*3731dup (SLC12A6) XP_011520569.1:n.*3731dup
XM_011522268.1:c.*3731dup (SLC12A6) XP_011520570.1:n.*3731dup
XR_429476.2:n.6406dup (SLC12A6)
NM_001351373.1:c.*368dup (EMC4) NP_001338302.1:n.*368dup
NM_001365088.1:c.*3731dup (SLC12A6) MANE Select NP_001352017.1:n.*3731dup
NR_147140.1:n.885dup (EMC4)
XM_006720793.4:c.*3731dup (SLC12A6) XP_006720856.1:n.*3731dup
NM_001042494.2:c.*3731dup (SLC12A6) NP_001035959.1:n.*3731dup
NM_001042495.2:c.*3731dup (SLC12A6) NP_001035960.1:n.*3731dup
NM_001042496.2:c.*3731dup (SLC12A6) NP_001035961.1:n.*3731dup
NM_001042497.2:c.*3731dup (SLC12A6) NP_001035962.1:n.*3731dup
NM_133647.2:c.*3731dup (SLC12A6) NP_598408.1:n.*3731dup