Canonical Allele Identifier: CA10518559

Gene: STK26

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.132054673C>T , CM000685.2:g.132054673C>T	GRCh38
NC_000023.10:g.131188701C>T , CM000685.1:g.131188701C>T	GRCh37
NC_000023.9:g.131016382C>T	NCBI36
NG_029562.1:g.36457C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_016542.4:c.85C>T MANE Select	NP_057626.2:p.Arg29Cys
ENST00000394334.7:c.85C>T MANE Select	ENSP00000377867.2:p.Arg29Cys
NM_001042452.1:c.85C>T	NP_001035917.1:p.Arg29Cys
NM_001042452.2:c.85C>T	NP_001035917.1:p.Arg29Cys
NM_001042453.1:c.43-8760C>T	NP_001035918.1:n.43-8760C>T
NM_001042453.2:c.43-8760C>T	NP_001035918.1:n.43-8760C>T
NM_016542.3:c.85C>T	NP_057626.2:p.Arg29Cys
ENST00000354719.10:c.85C>T	ENSP00000346755.6:p.Arg29Cys
ENST00000394334.6:c.85C>T	ENSP00000377867.2:p.Arg29Cys
ENST00000394335.6:c.43-8760C>T	ENSP00000377868.2:n.43-8760C>T
ENST00000481105.5:c.85C>T	ENSP00000418753.1:p.Arg29Cys
ENST00000496850.1:c.85C>T	ENSP00000419702.1:p.Arg29Cys
XM_011531349.1:c.-210C>T	XP_011529651.1:n.-210C>T
XM_011531350.1:c.-344C>T	XP_011529652.1:n.-344C>T