Canonical Allele Identifier: CA392044610

Gene: CDAN1

Linked Data

• MyVariant Identifiers: chr15:g.43023443T>G (hg19) ; chr15:g.42731245T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42731245T>G , CM000677.2:g.42731245T>G	GRCh38
NC_000015.9:g.43023443T>G , CM000677.1:g.43023443T>G	GRCh37
NC_000015.8:g.40810735T>G	NCBI36
NG_012491.1:g.10975A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356231.4:c.1826A>C MANE Select	ENSP00000348564.3:p.Asn609Thr
ENST00000643434.1:c.*1004A>C	ENSP00000494699.1:n.*1004A>C
ENST00000356231.3:c.1826A>C	ENSP00000348564.3:p.Asn609Thr
NM_138477.2:c.1826A>C	NP_612486.2:p.Asn609Thr
XM_005254176.3:c.1829A>C	XP_005254233.1:p.Asn610Thr
XM_011521270.1:c.1853A>C	XP_011519572.1:p.Asn618Thr
XM_011521271.1:c.1850A>C	XP_011519573.1:p.Asn617Thr
XM_011521272.1:c.1853A>C	XP_011519574.1:p.Asn618Thr
XM_011521273.1:c.1853A>C	XP_011519575.1:p.Asn618Thr
XM_011521274.1:c.818A>C	XP_011519576.1:p.Asn273Thr
XM_011521275.1:c.1070A>C	XP_011519577.1:p.Asn357Thr
XR_931757.1:n.1864A>C
NM_138477.4:c.1826A>C MANE Select	NP_612486.2:p.Asn609Thr
XM_005254176.5:c.1829A>C	XP_005254233.1:p.Asn610Thr
XM_011521270.2:c.1853A>C	XP_011519572.1:p.Asn618Thr
XM_011521271.2:c.1850A>C	XP_011519573.1:p.Asn617Thr
XM_011521274.2:c.818A>C	XP_011519576.1:p.Asn273Thr
XR_001751104.1:n.1883A>C
XR_001751105.1:n.1883A>C
XR_931757.2:n.1884A>C