Canonical Allele Identifier: CA1674230095

Gene: CNKSR3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.154405854G= , CM000668.2:g.154405854G=	GRCh38
NC_000006.11:g.154726988G= , CM000668.1:g.154726988G=	GRCh37
NC_000006.10:g.154768680G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607772.6:c.*500C= MANE Select	ENSP00000475915.1:n.*500C=
ENST00000673182.1:c.1369+4489C=	ENSP00000499846.1:n.1369+4489C=
ENST00000433165.6:n.1956C=
ENST00000607772.5:c.*500C=	ENSP00000475915.1:n.*500C=
ENST00000616478.4:c.1369+4489C=	ENSP00000478800.1:n.1369+4489C=
NM_173515.2:c.*500C=	NP_775786.2:n.*500C=
XM_011535485.1:c.*500C=	XP_011533787.1:n.*500C=
NM_173515.3:c.*500C=	NP_775786.2:n.*500C=
XM_011535485.3:c.*500C=	XP_011533787.1:n.*500C=
NM_173515.4:c.*500C= MANE Select	NP_775786.2:n.*500C=
NM_001368116.1:c.*500C=	NP_001355045.1:n.*500C=
NM_001368117.1:c.*508C=	NP_001355046.1:n.*508C=
NM_001368118.1:c.*500C=	NP_001355047.1:n.*500C=
NM_001368119.1:c.*500C=	NP_001355048.1:n.*500C=