Canonical Allele Identifier: CA1665339619
Gene: SGK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.134223595G= , CM000668.2:g.134223595G= GRCh38
NC_000006.11:g.134544733G= , CM000668.1:g.134544733G= GRCh37
NC_000006.10:g.134586426G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000367858.10:c.286-16164C= MANE Select ENSP00000356832.5:n.286-16164C=
ENST00000367858.9:c.286-16164C= ENSP00000356832.5:n.286-16164C=
ENST00000460769.1:c.128-8502C=
ENST00000461976.2:c.193-16164C= ENSP00000435577.1:n.193-16164C=
ENST00000484353.1:n.86-16164C=
ENST00000485771.1:n.83-4823C=
ENST00000524387.5:n.68+6805C=
ENST00000531575.5:n.86-16164C=
NM_001143676.1:c.286-16164C= NP_001137148.1:n.286-16164C=
XM_011536071.1:c.286-16164C= XP_011534373.1:n.286-16164C=
XR_001744360.2:n.344-4823C=
NM_001143676.3:c.286-16164C= MANE Select NP_001137148.1:n.286-16164C=