Canonical Allele Identifier: CA392037088

Gene: CDAN1

Linked Data

• MyVariant Identifiers: chr15:g.43021273T>G (hg19) ; chr15:g.42729075T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42729075T>G , CM000677.2:g.42729075T>G	GRCh38
NC_000015.9:g.43021273T>G , CM000677.1:g.43021273T>G	GRCh37
NC_000015.8:g.40808565T>G	NCBI36
NG_012491.1:g.13145A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000356231.4:c.2593A>C MANE Select	ENSP00000348564.3:p.Thr865Pro
ENST00000643434.1:c.*1771A>C	ENSP00000494699.1:n.*1771A>C
ENST00000356231.3:c.2593A>C	ENSP00000348564.3:p.Thr865Pro
ENST00000562465.5:c.586A>C	ENSP00000454246.1:p.Thr196Pro
NM_138477.2:c.2593A>C	NP_612486.2:p.Thr865Pro
XM_005254176.3:c.2596A>C	XP_005254233.1:p.Thr866Pro
XM_011521270.1:c.2620A>C	XP_011519572.1:p.Thr874Pro
XM_011521271.1:c.2617A>C	XP_011519573.1:p.Thr873Pro
XM_011521272.1:c.2620A>C	XP_011519574.1:p.Thr874Pro
XM_011521273.1:c.2620A>C	XP_011519575.1:p.Thr874Pro
XM_011521274.1:c.1585A>C	XP_011519576.1:p.Thr529Pro
XM_011521275.1:c.1837A>C	XP_011519577.1:p.Thr613Pro
NM_138477.4:c.2593A>C MANE Select	NP_612486.2:p.Thr865Pro
XM_005254176.5:c.2596A>C	XP_005254233.1:p.Thr866Pro
XM_011521270.2:c.2620A>C	XP_011519572.1:p.Thr874Pro
XM_011521271.2:c.2617A>C	XP_011519573.1:p.Thr873Pro
XM_011521274.2:c.1585A>C	XP_011519576.1:p.Thr529Pro
XR_001751104.1:n.2650A>C
XR_001751105.1:n.2650A>C