Canonical Allele Identifier: CA2695223670

Gene: SLC12A3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56870158_56870160del , CM000678.2:g.56870158_56870160del	GRCh38
NC_000016.9:g.56904070_56904072del , CM000678.1:g.56904070_56904072del	GRCh37
NC_000016.8:g.55461571_55461573del	NCBI36
NG_009386.1:g.9952_9954del
NG_009386.2:g.9952_9954del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563236.6:c.664_666del MANE Select	ENSP00000456149.2:p.Ile222del
ENST00000262502.5:c.661_663del	ENSP00000262502.5:p.Ile221del
ENST00000438926.6:c.664_666del	ENSP00000402152.2:p.Ile222del
ENST00000563236.5:c.664_666del	ENSP00000456149.1:p.Ile222del
ENST00000566786.5:c.661_663del	ENSP00000457552.1:p.Ile221del
NM_000339.2:c.664_666del	NP_000330.2:p.Ile222del
NM_001126107.1:c.661_663del	NP_001119579.1:p.Ile221del
NM_001126108.1:c.664_666del	NP_001119580.1:p.Ile222del
XM_005256119.1:c.661_663del	XP_005256176.1:p.Ile221del
XM_005256119.2:c.661_663del	XP_005256176.1:p.Ile221del
NM_000339.3:c.664_666del	NP_000330.3:p.Ile222del
NM_001126107.2:c.661_663del	NP_001119579.2:p.Ile221del
NM_001126108.2:c.664_666del MANE Select	NP_001119580.2:p.Ile222del