Canonical Allele Identifier: CA2175405943
Gene: SLC12A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48234885T= , CM000677.2:g.48234885T= GRCh38
NC_000015.9:g.48527082T= , CM000677.1:g.48527082T= GRCh37
NC_000015.8:g.46314374T= NCBI36
NG_021301.1:g.33585T=

Transcript Alleles

HGVS Amino-acid change
ENST00000686073.1:c.1096T= ENSP00000508901.1:p.Phe366=
ENST00000380993.8:c.1096T= MANE Select ENSP00000370381.3:p.Phe366=
ENST00000646012.1:c.1234T= ENSP00000495813.1:p.Phe412=
ENST00000647232.1:c.1096T= ENSP00000493875.1:p.Phe366=
ENST00000647546.1:c.1096T= ENSP00000495332.1:p.Phe366=
ENST00000330289.10:c.1096T= ENSP00000331550.6:p.Phe366=
ENST00000380993.7:c.1096T= ENSP00000370381.3:p.Phe366=
ENST00000396577.7:c.1096T= ENSP00000379822.3:p.Phe366=
ENST00000558252.5:n.5219T=
ENST00000558405.5:c.1096T= ENSP00000453409.1:p.Phe366=
ENST00000558805.1:c.123T=
ENST00000559641.5:c.535T= ENSP00000453230.1:p.Phe179=
ENST00000559723.2:n.469T=
ENST00000560692.5:n.5235T=
NM_000338.2:c.1096T= NP_000329.2:p.Phe366=
NM_001184832.1:c.1096T= NP_001171761.1:p.Phe366=
XM_005254605.1:c.1192T= XP_005254662.1:p.Phe398=
XM_005254606.1:c.1096T= XP_005254663.1:p.Phe366=
XM_006720656.1:c.1192T= XP_006720719.1:p.Phe398=
XR_931896.1:n.1408T=
XM_005254606.2:c.1096T= XP_005254663.1:p.Phe366=
NM_000338.3:c.1096T= MANE Select NP_000329.2:p.Phe366=
NM_001184832.2:c.1096T= NP_001171761.1:p.Phe366=
NM_001384136.1:c.1096T= NP_001371065.1:p.Phe366=