Canonical Allele Identifier: CA392307301
Gene: SLC12A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48229324T>A , CM000677.2:g.48229324T>A GRCh38
NC_000015.9:g.48521521T>A , CM000677.1:g.48521521T>A GRCh37
NC_000015.8:g.46308813T>A NCBI36
NG_021301.1:g.28024T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000686073.1:c.860T>A ENSP00000508901.1:p.Leu287His
ENST00000380993.8:c.860T>A MANE Select ENSP00000370381.3:p.Leu287His
ENST00000646012.1:c.998T>A ENSP00000495813.1:p.Leu333His
ENST00000647232.1:c.860T>A ENSP00000493875.1:p.Leu287His
ENST00000647546.1:c.860T>A ENSP00000495332.1:p.Leu287His
ENST00000330289.10:c.860T>A ENSP00000331550.6:p.Leu287His
ENST00000380993.7:c.860T>A ENSP00000370381.3:p.Leu287His
ENST00000396577.7:c.860T>A ENSP00000379822.3:p.Leu287His
ENST00000558252.5:n.4983T>A
ENST00000558405.5:c.860T>A ENSP00000453409.1:p.Leu287His
ENST00000559641.5:c.299T>A ENSP00000453230.1:p.Leu100His
ENST00000559723.2:n.233T>A
ENST00000560692.5:n.4999T>A
ENST00000561127.5:c.299T>A ENSP00000453602.2:p.Leu100His
NM_000338.2:c.860T>A NP_000329.2:p.Leu287His
NM_001184832.1:c.860T>A NP_001171761.1:p.Leu287His
XM_005254605.1:c.956T>A XP_005254662.1:p.Leu319His
XM_005254606.1:c.860T>A XP_005254663.1:p.Leu287His
XM_006720656.1:c.956T>A XP_006720719.1:p.Leu319His
XR_931896.1:n.1172T>A
XR_932203.1:n.229+632A>T
XR_932204.1:n.222+632A>T
XM_005254606.2:c.860T>A XP_005254663.1:p.Leu287His
XR_001751524.2:n.230+632A>T
XR_001751525.1:n.230+632A>T
XR_002957762.1:n.230+632A>T
XR_932204.3:n.224+632A>T
NM_000338.3:c.860T>A MANE Select NP_000329.2:p.Leu287His
NM_001184832.2:c.860T>A NP_001171761.1:p.Leu287His
NM_001384136.1:c.860T>A NP_001371065.1:p.Leu287His