Canonical Allele Identifier: CA2633375715
Gene: SLC12A3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56902515_56902516insAGG , CM000678.2:g.56902515_56902516insAGG GRCh38
NC_000016.9:g.56936427_56936428insAGG , CM000678.1:g.56936427_56936428insAGG GRCh37
NC_000016.8:g.55493928_55493929insAGG NCBI36
NG_009386.1:g.42309_42310insAGG
NG_009386.2:g.42309_42310insAGG

Transcript Alleles

HGVS Amino-acid change
ENST00000563236.6:c.2856+7_2856+8insAGG MANE Select ENSP00000456149.2:n.2856+7_2856+8insAGG
ENST00000262502.5:c.2853+7_2853+8insAGG ENSP00000262502.5:n.2853+7_2853+8insAGG
ENST00000438926.6:c.2883+7_2883+8insAGG ENSP00000402152.2:n.2883+7_2883+8insAGG
ENST00000563236.5:c.2856+7_2856+8insAGG ENSP00000456149.1:n.2856+7_2856+8insAGG
ENST00000566786.5:c.2880+7_2880+8insAGG ENSP00000457552.1:n.2880+7_2880+8insAGG
ENST00000569002.1:n.287+7_287+8insAGG
NM_000339.2:c.2883+7_2883+8insAGG NP_000330.2:n.2883+7_2883+8insAGG
NM_001126107.1:c.2880+7_2880+8insAGG NP_001119579.1:n.2880+7_2880+8insAGG
NM_001126108.1:c.2856+7_2856+8insAGG NP_001119580.1:n.2856+7_2856+8insAGG
XM_005256119.1:c.2853+7_2853+8insAGG XP_005256176.1:n.2853+7_2853+8insAGG
XM_005256119.2:c.2853+7_2853+8insAGG XP_005256176.1:n.2853+7_2853+8insAGG
NM_000339.3:c.2883+7_2883+8insAGG NP_000330.3:n.2883+7_2883+8insAGG
NM_001126107.2:c.2880+7_2880+8insAGG NP_001119579.2:n.2880+7_2880+8insAGG
NM_001126108.2:c.2856+7_2856+8insAGG MANE Select NP_001119580.2:n.2856+7_2856+8insAGG