Canonical Allele Identifier: CA2175405962
Gene: SLC12A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48234931T= , CM000677.2:g.48234931T= GRCh38
NC_000015.9:g.48527128T= , CM000677.1:g.48527128T= GRCh37
NC_000015.8:g.46314420T= NCBI36
NG_021301.1:g.33631T=

Transcript Alleles

HGVS Amino-acid change
ENST00000686073.1:c.1142T= ENSP00000508901.1:p.Phe381=
ENST00000380993.8:c.1142T= MANE Select ENSP00000370381.3:p.Phe381=
ENST00000646012.1:c.1280T= ENSP00000495813.1:p.Phe427=
ENST00000647232.1:c.1142T= ENSP00000493875.1:p.Phe381=
ENST00000647546.1:c.1142T= ENSP00000495332.1:p.Phe381=
ENST00000330289.10:c.1142T= ENSP00000331550.6:p.Phe381=
ENST00000380993.7:c.1142T= ENSP00000370381.3:p.Phe381=
ENST00000396577.7:c.1142T= ENSP00000379822.3:p.Phe381=
ENST00000558252.5:n.5265T=
ENST00000558405.5:c.1142T= ENSP00000453409.1:p.Phe381=
ENST00000558805.1:c.169T=
ENST00000559641.5:c.581T= ENSP00000453230.1:p.Phe194=
ENST00000560692.5:n.5281T=
NM_000338.2:c.1142T= NP_000329.2:p.Phe381=
NM_001184832.1:c.1142T= NP_001171761.1:p.Phe381=
XM_005254605.1:c.1238T= XP_005254662.1:p.Phe413=
XM_005254606.1:c.1142T= XP_005254663.1:p.Phe381=
XM_006720656.1:c.1238T= XP_006720719.1:p.Phe413=
XR_931896.1:n.1454T=
XM_005254606.2:c.1142T= XP_005254663.1:p.Phe381=
NM_000338.3:c.1142T= MANE Select NP_000329.2:p.Phe381=
NM_001184832.2:c.1142T= NP_001171761.1:p.Phe381=
NM_001384136.1:c.1142T= NP_001371065.1:p.Phe381=