Canonical Allele Identifier: CA392307313
Gene: SLC12A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48229327A>T , CM000677.2:g.48229327A>T GRCh38
NC_000015.9:g.48521524A>T , CM000677.1:g.48521524A>T GRCh37
NC_000015.8:g.46308816A>T NCBI36
NG_021301.1:g.28027A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000686073.1:c.863A>T ENSP00000508901.1:p.Lys288Met
ENST00000380993.8:c.863A>T MANE Select ENSP00000370381.3:p.Lys288Met
ENST00000646012.1:c.1001A>T ENSP00000495813.1:p.Lys334Met
ENST00000647232.1:c.863A>T ENSP00000493875.1:p.Lys288Met
ENST00000647546.1:c.863A>T ENSP00000495332.1:p.Lys288Met
ENST00000330289.10:c.863A>T ENSP00000331550.6:p.Lys288Met
ENST00000380993.7:c.863A>T ENSP00000370381.3:p.Lys288Met
ENST00000396577.7:c.863A>T ENSP00000379822.3:p.Lys288Met
ENST00000558252.5:n.4986A>T
ENST00000558405.5:c.863A>T ENSP00000453409.1:p.Lys288Met
ENST00000559641.5:c.302A>T ENSP00000453230.1:p.Lys101Met
ENST00000559723.2:n.236A>T
ENST00000560692.5:n.5002A>T
ENST00000561127.5:c.302A>T ENSP00000453602.2:p.Lys101Met
NM_000338.2:c.863A>T NP_000329.2:p.Lys288Met
NM_001184832.1:c.863A>T NP_001171761.1:p.Lys288Met
XM_005254605.1:c.959A>T XP_005254662.1:p.Lys320Met
XM_005254606.1:c.863A>T XP_005254663.1:p.Lys288Met
XM_006720656.1:c.959A>T XP_006720719.1:p.Lys320Met
XR_931896.1:n.1175A>T
XR_932203.1:n.229+629T>A
XR_932204.1:n.222+629T>A
XM_005254606.2:c.863A>T XP_005254663.1:p.Lys288Met
XR_001751524.2:n.230+629T>A
XR_001751525.1:n.230+629T>A
XR_002957762.1:n.230+629T>A
XR_932204.3:n.224+629T>A
NM_000338.3:c.863A>T MANE Select NP_000329.2:p.Lys288Met
NM_001184832.2:c.863A>T NP_001171761.1:p.Lys288Met
NM_001384136.1:c.863A>T NP_001371065.1:p.Lys288Met