Canonical Allele Identifier: CA392307119
Gene: SLC12A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48229285T>A , CM000677.2:g.48229285T>A GRCh38
NC_000015.9:g.48521482T>A , CM000677.1:g.48521482T>A GRCh37
NC_000015.8:g.46308774T>A NCBI36
NG_021301.1:g.27985T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000686073.1:c.821T>A ENSP00000508901.1:p.Met274Lys
ENST00000380993.8:c.821T>A MANE Select ENSP00000370381.3:p.Met274Lys
ENST00000646012.1:c.959T>A ENSP00000495813.1:p.Met320Lys
ENST00000647232.1:c.821T>A ENSP00000493875.1:p.Met274Lys
ENST00000647546.1:c.821T>A ENSP00000495332.1:p.Met274Lys
ENST00000330289.10:c.821T>A ENSP00000331550.6:p.Met274Lys
ENST00000380993.7:c.821T>A ENSP00000370381.3:p.Met274Lys
ENST00000396577.7:c.821T>A ENSP00000379822.3:p.Met274Lys
ENST00000558252.5:n.4944T>A
ENST00000558405.5:c.821T>A ENSP00000453409.1:p.Met274Lys
ENST00000559641.5:c.260T>A ENSP00000453230.1:p.Met87Lys
ENST00000559723.2:n.194T>A
ENST00000560692.5:n.4960T>A
ENST00000561127.5:c.260T>A ENSP00000453602.2:p.Met87Lys
NM_000338.2:c.821T>A NP_000329.2:p.Met274Lys
NM_001184832.1:c.821T>A NP_001171761.1:p.Met274Lys
XM_005254605.1:c.917T>A XP_005254662.1:p.Met306Lys
XM_005254606.1:c.821T>A XP_005254663.1:p.Met274Lys
XM_006720656.1:c.917T>A XP_006720719.1:p.Met306Lys
XR_931896.1:n.1133T>A
XR_932203.1:n.229+671A>T
XR_932204.1:n.222+671A>T
XM_005254606.2:c.821T>A XP_005254663.1:p.Met274Lys
XR_001751524.2:n.230+671A>T
XR_001751525.1:n.230+671A>T
XR_002957762.1:n.230+671A>T
XR_932204.3:n.224+671A>T
NM_000338.3:c.821T>A MANE Select NP_000329.2:p.Met274Lys
NM_001184832.2:c.821T>A NP_001171761.1:p.Met274Lys
NM_001384136.1:c.821T>A NP_001371065.1:p.Met274Lys