Canonical Allele Identifier: CA392044887

Gene: CDAN1

Linked Data

• MyVariant Identifiers: chr15:g.43023473T>A (hg19) ; chr15:g.42731275T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42731275T>A , CM000677.2:g.42731275T>A	GRCh38
NC_000015.9:g.43023473T>A , CM000677.1:g.43023473T>A	GRCh37
NC_000015.8:g.40810765T>A	NCBI36
NG_012491.1:g.10945A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000356231.4:c.1796A>T MANE Select	ENSP00000348564.3:p.Asn599Ile
ENST00000643434.1:c.*974A>T	ENSP00000494699.1:n.*974A>T
ENST00000356231.3:c.1796A>T	ENSP00000348564.3:p.Asn599Ile
NM_138477.2:c.1796A>T	NP_612486.2:p.Asn599Ile
XM_005254176.3:c.1799A>T	XP_005254233.1:p.Asn600Ile
XM_011521270.1:c.1823A>T	XP_011519572.1:p.Asn608Ile
XM_011521271.1:c.1820A>T	XP_011519573.1:p.Asn607Ile
XM_011521272.1:c.1823A>T	XP_011519574.1:p.Asn608Ile
XM_011521273.1:c.1823A>T	XP_011519575.1:p.Asn608Ile
XM_011521274.1:c.788A>T	XP_011519576.1:p.Asn263Ile
XM_011521275.1:c.1040A>T	XP_011519577.1:p.Asn347Ile
XR_931757.1:n.1834A>T
NM_138477.4:c.1796A>T MANE Select	NP_612486.2:p.Asn599Ile
XM_005254176.5:c.1799A>T	XP_005254233.1:p.Asn600Ile
XM_011521270.2:c.1823A>T	XP_011519572.1:p.Asn608Ile
XM_011521271.2:c.1820A>T	XP_011519573.1:p.Asn607Ile
XM_011521274.2:c.788A>T	XP_011519576.1:p.Asn263Ile
XR_001751104.1:n.1853A>T
XR_001751105.1:n.1853A>T
XR_931757.2:n.1854A>T