Canonical Allele Identifier: CA2633377815
Gene: SLC12A3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56902531_56902532insGCCCC , CM000678.2:g.56902531_56902532insGCCCC GRCh38
NC_000016.9:g.56936443_56936444insGCCCC , CM000678.1:g.56936443_56936444insGCCCC GRCh37
NC_000016.8:g.55493944_55493945insGCCCC NCBI36
NG_009386.1:g.42325_42326insGCCCC
NG_009386.2:g.42325_42326insGCCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000563236.6:c.2856+23_2856+24insGCCCC MANE Select ENSP00000456149.2:n.2856+23_2856+24insGCCCC
ENST00000262502.5:c.2853+23_2853+24insGCCCC ENSP00000262502.5:n.2853+23_2853+24insGCCCC
ENST00000438926.6:c.2883+23_2883+24insGCCCC ENSP00000402152.2:n.2883+23_2883+24insGCCCC
ENST00000563236.5:c.2856+23_2856+24insGCCCC ENSP00000456149.1:n.2856+23_2856+24insGCCCC
ENST00000566786.5:c.2880+23_2880+24insGCCCC ENSP00000457552.1:n.2880+23_2880+24insGCCCC
ENST00000569002.1:n.287+23_287+24insGCCCC
NM_000339.2:c.2883+23_2883+24insGCCCC NP_000330.2:n.2883+23_2883+24insGCCCC
NM_001126107.1:c.2880+23_2880+24insGCCCC NP_001119579.1:n.2880+23_2880+24insGCCCC
NM_001126108.1:c.2856+23_2856+24insGCCCC NP_001119580.1:n.2856+23_2856+24insGCCCC
XM_005256119.1:c.2853+23_2853+24insGCCCC XP_005256176.1:n.2853+23_2853+24insGCCCC
XM_005256119.2:c.2853+23_2853+24insGCCCC XP_005256176.1:n.2853+23_2853+24insGCCCC
NM_000339.3:c.2883+23_2883+24insGCCCC NP_000330.3:n.2883+23_2883+24insGCCCC
NM_001126107.2:c.2880+23_2880+24insGCCCC NP_001119579.2:n.2880+23_2880+24insGCCCC
NM_001126108.2:c.2856+23_2856+24insGCCCC MANE Select NP_001119580.2:n.2856+23_2856+24insGCCCC