Canonical Allele Identifier: CA396002172
Gene: SLC12A3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56904395T>A , CM000678.2:g.56904395T>A GRCh38
NC_000016.9:g.56938307T>A , CM000678.1:g.56938307T>A GRCh37
NC_000016.8:g.55495808T>A NCBI36
NG_009386.1:g.44189T>A
NG_009386.2:g.44189T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000563236.6:c.2857T>A MANE Select ENSP00000456149.2:p.Ser953Thr
ENST00000262502.5:c.2854T>A ENSP00000262502.5:p.Ser952Thr
ENST00000438926.6:c.2884T>A ENSP00000402152.2:p.Ser962Thr
ENST00000563236.5:c.2857T>A ENSP00000456149.1:p.Ser953Thr
ENST00000566786.5:c.2881T>A ENSP00000457552.1:p.Ser961Thr
ENST00000569002.1:n.288T>A
NM_000339.2:c.2884T>A NP_000330.2:p.Ser962Thr
NM_001126107.1:c.2881T>A NP_001119579.1:p.Ser961Thr
NM_001126108.1:c.2857T>A NP_001119580.1:p.Ser953Thr
XM_005256119.1:c.2854T>A XP_005256176.1:p.Ser952Thr
XM_005256119.2:c.2854T>A XP_005256176.1:p.Ser952Thr
NM_000339.3:c.2884T>A NP_000330.3:p.Ser962Thr
NM_001126107.2:c.2881T>A NP_001119579.2:p.Ser961Thr
NM_001126108.2:c.2857T>A MANE Select NP_001119580.2:p.Ser953Thr