Canonical Allele Identifier: CA2175415698
Gene: SLC12A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48246889C= , CM000677.2:g.48246889C= GRCh38
NC_000015.9:g.48539086C= , CM000677.1:g.48539086C= GRCh37
NC_000015.8:g.46326378C= NCBI36
NG_021301.1:g.45589C=

Transcript Alleles

HGVS Amino-acid change
ENST00000686073.1:c.1453-20C= ENSP00000508901.1:n.1453-20C=
ENST00000380993.8:c.1453-20C= MANE Select ENSP00000370381.3:n.1453-20C=
ENST00000646012.1:c.1591-20C= ENSP00000495813.1:n.1591-20C=
ENST00000647232.1:c.1453-20C= ENSP00000493875.1:n.1453-20C=
ENST00000647546.1:c.1453-20C= ENSP00000495332.1:n.1453-20C=
ENST00000380993.7:c.1453-20C= ENSP00000370381.3:n.1453-20C=
ENST00000396577.7:c.1453-20C= ENSP00000379822.3:n.1453-20C=
ENST00000558252.5:n.5576-20C=
ENST00000558405.5:c.1453-20C= ENSP00000453409.1:n.1453-20C=
ENST00000559641.5:c.892-20C= ENSP00000453230.1:n.892-20C=
ENST00000560692.5:n.5592-20C=
NM_000338.2:c.1453-20C= NP_000329.2:n.1453-20C=
NM_001184832.1:c.1453-20C= NP_001171761.1:n.1453-20C=
XM_005254605.1:c.1549-20C= XP_005254662.1:n.1549-20C=
XM_005254606.1:c.1453-20C= XP_005254663.1:n.1453-20C=
XM_006720656.1:c.1549-20C= XP_006720719.1:n.1549-20C=
XR_931896.1:n.1765-20C=
XM_005254606.2:c.1453-20C= XP_005254663.1:n.1453-20C=
XR_001751535.1:n.88-4462G=
NM_000338.3:c.1453-20C= MANE Select NP_000329.2:n.1453-20C=
NM_001184832.2:c.1453-20C= NP_001171761.1:n.1453-20C=
NM_001384136.1:c.1453-20C= NP_001371065.1:n.1453-20C=