Canonical Allele Identifier: CA2224361235
Gene: SLC12A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56894585G= , CM000678.2:g.56894585G= GRCh38
NC_000016.9:g.56928497G= , CM000678.1:g.56928497G= GRCh37
NC_000016.8:g.55485998G= NCBI36
NG_009386.1:g.34379G=
NG_009386.2:g.34379G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000563236.6:c.2576G= MANE Select ENSP00000456149.2:p.Cys859=
ENST00000262502.5:c.2573G= ENSP00000262502.5:p.Cys858=
ENST00000438926.6:c.2603G= ENSP00000402152.2:p.Cys868=
ENST00000563236.5:c.2576G= ENSP00000456149.1:p.Cys859=
ENST00000566786.5:c.2600G= ENSP00000457552.1:p.Cys867=
NM_000339.2:c.2603G= NP_000330.2:p.Cys868=
NM_001126107.1:c.2600G= NP_001119579.1:p.Cys867=
NM_001126108.1:c.2576G= NP_001119580.1:p.Cys859=
XM_005256119.1:c.2573G= XP_005256176.1:p.Cys858=
XM_005256119.2:c.2573G= XP_005256176.1:p.Cys858=
NM_000339.3:c.2603G= NP_000330.3:p.Cys868=
NM_001126107.2:c.2600G= NP_001119579.2:p.Cys867=
NM_001126108.2:c.2576G= MANE Select NP_001119580.2:p.Cys859=