Canonical Allele Identifier: CA2633375859

Gene: SLC12A3

Linked Data

• gnomAD v4: 16-56902522-T-TGGGGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56902527_56902528insGGGGGG , CM000678.2:g.56902527_56902528insGGGGGG	GRCh38
NC_000016.9:g.56936439_56936440insGGGGGG , CM000678.1:g.56936439_56936440insGGGGGG	GRCh37
NC_000016.8:g.55493940_55493941insGGGGGG	NCBI36
NG_009386.1:g.42321_42322insGGGGGG
NG_009386.2:g.42321_42322insGGGGGG

Transcript Alleles

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