Canonical Allele Identifier: CA4062662

Gene: CNKSR3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.154450098T>A , CM000668.2:g.154450098T>A	GRCh38
NC_000006.11:g.154771232T>A , CM000668.1:g.154771232T>A	GRCh37
NC_000006.10:g.154812924T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_173515.4:c.213A>T MANE Select	NP_775786.2:p.Ala71=
ENST00000607772.6:c.213A>T MANE Select	ENSP00000475915.1:p.Ala71=
NM_001368116.1:c.231A>T	NP_001355045.1:p.Ala77=
NM_001368117.1:c.213A>T	NP_001355046.1:p.Ala71=
NM_001368118.1:c.-28A>T	NP_001355047.1:n.-28A>T
NM_173515.2:c.213A>T	NP_775786.2:p.Ala71=
NM_173515.3:c.213A>T	NP_775786.2:p.Ala71=
ENST00000479339.5:c.-28A>T	ENSP00000418975.1:n.-28A>T
ENST00000607772.5:c.213A>T	ENSP00000475915.1:p.Ala71=
ENST00000616478.4:c.213A>T	ENSP00000478800.1:p.Ala71=
ENST00000673182.1:c.213A>T	ENSP00000499846.1:p.Ala71=
XM_011535485.1:c.183A>T	XP_011533787.1:p.Ala61=
XM_011535485.3:c.183A>T	XP_011533787.1:p.Ala61=