Canonical Allele Identifier: CA365725596

Gene: SGK1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.134170860T>C , CM000668.2:g.134170860T>C	GRCh38
NC_000006.11:g.134491998T>C , CM000668.1:g.134491998T>C	GRCh37
NC_000006.10:g.134533691T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001143676.3:c.1379A>G MANE Select	NP_001137148.1:p.Asn460Ser
ENST00000367858.10:c.1379A>G MANE Select	ENSP00000356832.5:p.Asn460Ser
NM_001143676.1:c.1379A>G	NP_001137148.1:p.Asn460Ser
NM_001143677.1:c.1178A>G	NP_001137149.1:p.Asn393Ser
NM_001143677.2:c.1178A>G	NP_001137149.1:p.Asn393Ser
NM_001143678.1:c.1136A>G	NP_001137150.1:p.Asn379Ser
NM_001143678.2:c.1136A>G	NP_001137150.1:p.Asn379Ser
NM_001291995.1:c.962A>G	NP_001278924.1:p.Asn321Ser
NM_001291995.2:c.962A>G	NP_001278924.1:p.Asn321Ser
NM_005627.3:c.1094A>G	NP_005618.2:p.Asn365Ser
NM_005627.4:c.1094A>G	NP_005618.2:p.Asn365Ser
ENST00000237305.11:c.1094A>G	ENSP00000237305.7:p.Asn365Ser
ENST00000237305.12:c.1094A>G	ENSP00000237305.7:p.Asn365Ser
ENST00000367855.7:n.1236A>G
ENST00000367857.9:c.1064A>G	ENSP00000356831.5:p.Asn355Ser
ENST00000367858.9:c.1379A>G	ENSP00000356832.5:p.Asn460Ser
ENST00000413996.7:c.1136A>G	ENSP00000396242.3:p.Asn379Ser
ENST00000474427.6:n.3862A>G
ENST00000475719.6:c.962A>G	ENSP00000434302.1:p.Asn321Ser
ENST00000477460.6:n.678A>G
ENST00000528577.5:c.1178A>G	ENSP00000434450.1:p.Asn393Ser
ENST00000531782.1:n.520A>G
XM_011536071.1:c.1379A>G	XP_011534373.1:p.Asn460Ser