Canonical Allele Identifier: CA2175420381
Gene: SLC12A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48251788T= , CM000677.2:g.48251788T= GRCh38
NC_000015.9:g.48543985T= , CM000677.1:g.48543985T= GRCh37
NC_000015.8:g.46331277T= NCBI36
NG_021301.1:g.50488T=

Transcript Alleles

HGVS Amino-acid change
ENST00000686073.1:c.1942+18T= ENSP00000508901.1:n.1942+18T=
ENST00000380993.8:c.1942+18T= MANE Select ENSP00000370381.3:n.1942+18T=
ENST00000646012.1:c.2080+18T= ENSP00000495813.1:n.2080+18T=
ENST00000647232.1:c.1942+18T= ENSP00000493875.1:n.1942+18T=
ENST00000647546.1:c.1942+18T= ENSP00000495332.1:n.1942+18T=
ENST00000380993.7:c.1942+18T= ENSP00000370381.3:n.1942+18T=
ENST00000396577.7:c.1942+18T= ENSP00000379822.3:n.1942+18T=
ENST00000558252.5:n.6065+18T=
ENST00000558405.5:c.1942+18T= ENSP00000453409.1:n.1942+18T=
ENST00000559641.5:c.1381+18T= ENSP00000453230.1:n.1381+18T=
ENST00000560692.5:n.6081+18T=
NM_000338.2:c.1942+18T= NP_000329.2:n.1942+18T=
NM_001184832.1:c.1942+18T= NP_001171761.1:n.1942+18T=
XM_005254605.1:c.2038+18T= XP_005254662.1:n.2038+18T=
XM_005254606.1:c.1942+18T= XP_005254663.1:n.1942+18T=
XM_006720656.1:c.2038+18T= XP_006720719.1:n.2038+18T=
XR_931896.1:n.2254+18T=
XM_005254606.2:c.1942+18T= XP_005254663.1:n.1942+18T=
NM_000338.3:c.1942+18T= MANE Select NP_000329.2:n.1942+18T=
NM_001184832.2:c.1942+18T= NP_001171761.1:n.1942+18T=
NM_001384136.1:c.1942+18T= NP_001371065.1:n.1942+18T=