Canonical Allele Identifier: CA1665390476
Gene: SGK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.134277935A= , CM000668.2:g.134277935A= GRCh38
NC_000006.11:g.134599073A= , CM000668.1:g.134599073A= GRCh37
NC_000006.10:g.134640766A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000367858.10:c.70-15787T= MANE Select ENSP00000356832.5:n.70-15787T=
ENST00000367858.9:c.70-15787T= ENSP00000356832.5:n.70-15787T=
ENST00000461976.2:c.-24-15787T= ENSP00000435577.1:n.-24-15787T=
ENST00000524929.1:c.70-15787T= ENSP00000435724.1:n.70-15787T=
ENST00000533224.1:c.70-15787T= ENSP00000436470.1:n.70-15787T=
NM_001143676.1:c.70-15787T= NP_001137148.1:n.70-15787T=
XM_011536071.1:c.70-15787T= XP_011534373.1:n.70-15787T=
NM_001143676.3:c.70-15787T= MANE Select NP_001137148.1:n.70-15787T=