Canonical Allele Identifier: CA2633375857
Gene: SLC12A3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56902527_56902528insGGAGGGGGGGGGGGGGG , CM000678.2:g.56902527_56902528insGGAGGGGGGGGGGGGGG GRCh38
NC_000016.9:g.56936439_56936440insGGAGGGGGGGGGGGGGG , CM000678.1:g.56936439_56936440insGGAGGGGGGGGGGGGGG GRCh37
NC_000016.8:g.55493940_55493941insGGAGGGGGGGGGGGGGG NCBI36
NG_009386.1:g.42321_42322insGGAGGGGGGGGGGGGGG
NG_009386.2:g.42321_42322insGGAGGGGGGGGGGGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000563236.6:c.2856+19_2856+20insGGAGGGGGGGGGGGGGG MANE Select ENSP00000456149.2:n.2856+19_2856+20insGGAGGGGGGGGGGGGGG
ENST00000262502.5:c.2853+19_2853+20insGGAGGGGGGGGGGGGGG ENSP00000262502.5:n.2853+19_2853+20insGGAGGGGGGGGGGGGGG
ENST00000438926.6:c.2883+19_2883+20insGGAGGGGGGGGGGGGGG ENSP00000402152.2:n.2883+19_2883+20insGGAGGGGGGGGGGGGGG
ENST00000563236.5:c.2856+19_2856+20insGGAGGGGGGGGGGGGGG ENSP00000456149.1:n.2856+19_2856+20insGGAGGGGGGGGGGGGGG
ENST00000566786.5:c.2880+19_2880+20insGGAGGGGGGGGGGGGGG ENSP00000457552.1:n.2880+19_2880+20insGGAGGGGGGGGGGGGGG
ENST00000569002.1:n.287+19_287+20insGGAGGGGGGGGGGGGGG
NM_000339.2:c.2883+19_2883+20insGGAGGGGGGGGGGGGGG NP_000330.2:n.2883+19_2883+20insGGAGGGGGGGGGGGGGG
NM_001126107.1:c.2880+19_2880+20insGGAGGGGGGGGGGGGGG NP_001119579.1:n.2880+19_2880+20insGGAGGGGGGGGGGGGGG
NM_001126108.1:c.2856+19_2856+20insGGAGGGGGGGGGGGGGG NP_001119580.1:n.2856+19_2856+20insGGAGGGGGGGGGGGGGG
XM_005256119.1:c.2853+19_2853+20insGGAGGGGGGGGGGGGGG XP_005256176.1:n.2853+19_2853+20insGGAGGGGGGGGGGGGGG
XM_005256119.2:c.2853+19_2853+20insGGAGGGGGGGGGGGGGG XP_005256176.1:n.2853+19_2853+20insGGAGGGGGGGGGGGGGG
NM_000339.3:c.2883+19_2883+20insGGAGGGGGGGGGGGGGG NP_000330.3:n.2883+19_2883+20insGGAGGGGGGGGGGGGGG
NM_001126107.2:c.2880+19_2880+20insGGAGGGGGGGGGGGGGG NP_001119579.2:n.2880+19_2880+20insGGAGGGGGGGGGGGGGG
NM_001126108.2:c.2856+19_2856+20insGGAGGGGGGGGGGGGGG MANE Select NP_001119580.2:n.2856+19_2856+20insGGAGGGGGGGGGGGGGG