Canonical Allele Identifier: CA2633377862

Gene: SLC12A3

Linked Data

• gnomAD v4: 16-56902531-G-GGGGGGGCCGCC

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56902531_56902532insGGGGGGCCGCC , CM000678.2:g.56902531_56902532insGGGGGGCCGCC	GRCh38
NC_000016.9:g.56936443_56936444insGGGGGGCCGCC , CM000678.1:g.56936443_56936444insGGGGGGCCGCC	GRCh37
NC_000016.8:g.55493944_55493945insGGGGGGCCGCC	NCBI36
NG_009386.1:g.42325_42326insGGGGGGCCGCC
NG_009386.2:g.42325_42326insGGGGGGCCGCC

Transcript Alleles

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