Canonical Allele Identifier: CA412553654

Gene: CNKSR2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.21648861C>T , CM000685.2:g.21648861C>T	GRCh38
NC_000023.10:g.21666979C>T , CM000685.1:g.21666979C>T	GRCh37
NC_000023.9:g.21576900C>T	NCBI36
NG_016266.1:g.279444C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_014927.5:c.2723C>T MANE Select	NP_055742.2:p.Ser908Leu
ENST00000379510.5:c.2723C>T MANE Select	ENSP00000368824.3:p.Ser908Leu
NM_001168647.1:c.2633C>T	NP_001162118.1:p.Ser878Leu
NM_001168647.2:c.2633C>T	NP_001162118.1:p.Ser878Leu
NM_001168647.3:c.2633C>T	NP_001162118.1:p.Ser878Leu
NM_001330770.1:c.2576C>T	NP_001317699.1:p.Ser859Leu
NM_001330770.2:c.2576C>T	NP_001317699.1:p.Ser859Leu
NM_001330772.1:c.2486C>T	NP_001317701.1:p.Ser829Leu
NM_001330772.2:c.2486C>T	NP_001317701.1:p.Ser829Leu
NM_014927.3:c.2723C>T	NP_055742.2:p.Ser908Leu
NM_014927.4:c.2723C>T	NP_055742.2:p.Ser908Leu
ENST00000379510.3:c.2723C>T	ENSP00000368824.3:p.Ser908Leu
ENST00000425654.6:c.2633C>T	ENSP00000397906.2:p.Ser878Leu
ENST00000425654.7:c.2633C>T	ENSP00000397906.2:p.Ser878Leu
ENST00000642853.1:n.2501C>T
ENST00000643156.1:c.1555C>T
ENST00000643484.1:n.2431C>T
ENST00000644075.1:n.2089C>T
ENST00000644295.1:c.2648C>T	ENSP00000495501.1:p.Ser883Leu
ENST00000644585.1:c.2576C>T	ENSP00000495954.1:p.Ser859Leu
ENST00000645238.1:n.552C>T
ENST00000645245.1:c.2486C>T	ENSP00000495695.1:p.Ser829Leu
ENST00000645539.1:n.920C>T
ENST00000646690.1:n.731C>T
ENST00000647532.1:n.6482C>T