Canonical Allele Identifier: CA2576002382

Gene: SLC12A3

Linked Data

• gnomAD v4: 16-56902528-TGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56902530_56902531del , CM000678.2:g.56902530_56902531del	GRCh38
NC_000016.9:g.56936442_56936443del , CM000678.1:g.56936442_56936443del	GRCh37
NC_000016.8:g.55493943_55493944del	NCBI36
NG_009386.1:g.42324_42325del
NG_009386.2:g.42324_42325del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563236.6:c.2856+22_2856+23del MANE Select	ENSP00000456149.2:n.2856+22_2856+23del
ENST00000262502.5:c.2853+22_2853+23del	ENSP00000262502.5:n.2853+22_2853+23del
ENST00000438926.6:c.2883+22_2883+23del	ENSP00000402152.2:n.2883+22_2883+23del
ENST00000563236.5:c.2856+22_2856+23del	ENSP00000456149.1:n.2856+22_2856+23del
ENST00000566786.5:c.2880+22_2880+23del	ENSP00000457552.1:n.2880+22_2880+23del
ENST00000569002.1:n.287+22_287+23del
NM_000339.2:c.2883+22_2883+23del	NP_000330.2:n.2883+22_2883+23del
NM_001126107.1:c.2880+22_2880+23del	NP_001119579.1:n.2880+22_2880+23del
NM_001126108.1:c.2856+22_2856+23del	NP_001119580.1:n.2856+22_2856+23del
XM_005256119.1:c.2853+22_2853+23del	XP_005256176.1:n.2853+22_2853+23del
XM_005256119.2:c.2853+22_2853+23del	XP_005256176.1:n.2853+22_2853+23del
NM_000339.3:c.2883+22_2883+23del	NP_000330.3:n.2883+22_2883+23del
NM_001126107.2:c.2880+22_2880+23del	NP_001119579.2:n.2880+22_2880+23del
NM_001126108.2:c.2856+22_2856+23del MANE Select	NP_001119580.2:n.2856+22_2856+23del