Canonical Allele Identifier: CA2175405965
Gene: SLC12A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48234934C= , CM000677.2:g.48234934C= GRCh38
NC_000015.9:g.48527131C= , CM000677.1:g.48527131C= GRCh37
NC_000015.8:g.46314423C= NCBI36
NG_021301.1:g.33634C=

Transcript Alleles

HGVS Amino-acid change
ENST00000686073.1:c.1145C= ENSP00000508901.1:p.Ser382=
ENST00000380993.8:c.1145C= MANE Select ENSP00000370381.3:p.Ser382=
ENST00000646012.1:c.1283C= ENSP00000495813.1:p.Ser428=
ENST00000647232.1:c.1145C= ENSP00000493875.1:p.Ser382=
ENST00000647546.1:c.1145C= ENSP00000495332.1:p.Ser382=
ENST00000330289.10:c.1145C= ENSP00000331550.6:p.Ser382=
ENST00000380993.7:c.1145C= ENSP00000370381.3:p.Ser382=
ENST00000396577.7:c.1145C= ENSP00000379822.3:p.Ser382=
ENST00000558252.5:n.5268C=
ENST00000558405.5:c.1145C= ENSP00000453409.1:p.Ser382=
ENST00000558805.1:c.172C=
ENST00000559641.5:c.584C= ENSP00000453230.1:p.Ser195=
ENST00000560692.5:n.5284C=
NM_000338.2:c.1145C= NP_000329.2:p.Ser382=
NM_001184832.1:c.1145C= NP_001171761.1:p.Ser382=
XM_005254605.1:c.1241C= XP_005254662.1:p.Ser414=
XM_005254606.1:c.1145C= XP_005254663.1:p.Ser382=
XM_006720656.1:c.1241C= XP_006720719.1:p.Ser414=
XR_931896.1:n.1457C=
XM_005254606.2:c.1145C= XP_005254663.1:p.Ser382=
NM_000338.3:c.1145C= MANE Select NP_000329.2:p.Ser382=
NM_001184832.2:c.1145C= NP_001171761.1:p.Ser382=
NM_001384136.1:c.1145C= NP_001371065.1:p.Ser382=