Canonical Allele Identifier: CA2628314711
Gene: SLC12A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48226519T>C , CM000677.2:g.48226519T>C GRCh38
NC_000015.9:g.48518716T>C , CM000677.1:g.48518716T>C GRCh37
NC_000015.8:g.46306008T>C NCBI36
NG_021301.1:g.25219T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000686073.1:c.724+572T>C ENSP00000508901.1:n.724+572T>C
ENST00000380993.8:c.672T>C MANE Select ENSP00000370381.3:p.Ser224=
ENST00000646012.1:c.810T>C ENSP00000495813.1:p.Ser270=
ENST00000647232.1:c.629-560T>C ENSP00000493875.1:n.629-560T>C
ENST00000647546.1:c.672T>C ENSP00000495332.1:p.Ser224=
ENST00000330289.10:c.672T>C ENSP00000331550.6:p.Ser224=
ENST00000380993.7:c.672T>C ENSP00000370381.3:p.Ser224=
ENST00000396577.7:c.629-560T>C ENSP00000379822.3:n.629-560T>C
ENST00000558252.5:n.4192T>C
ENST00000558405.5:c.672T>C ENSP00000453409.1:p.Ser224=
ENST00000559641.5:c.111T>C ENSP00000453230.1:p.Ser37=
ENST00000559723.2:n.97+572T>C
ENST00000560692.5:n.2194T>C
ENST00000561127.5:c.111T>C ENSP00000453602.2:p.Ser37=
NM_000338.2:c.672T>C NP_000329.2:p.Ser224=
NM_001184832.1:c.629-560T>C NP_001171761.1:n.629-560T>C
XM_005254605.1:c.672T>C XP_005254662.1:p.Ser224=
XM_005254606.1:c.724+572T>C XP_005254663.1:n.724+572T>C
XM_006720656.1:c.672T>C XP_006720719.1:p.Ser224=
XR_931896.1:n.888T>C
XM_005254606.2:c.724+572T>C XP_005254663.1:n.724+572T>C
XR_001751524.2:n.363+942A>G
XR_001751525.1:n.363+942A>G
XR_002957762.1:n.363+942A>G
XR_932204.3:n.357+942A>G
NM_000338.3:c.672T>C MANE Select NP_000329.2:p.Ser224=
NM_001184832.2:c.629-560T>C NP_001171761.1:n.629-560T>C
NM_001384136.1:c.724+572T>C NP_001371065.1:n.724+572T>C