Canonical Allele Identifier: CA392045240

Gene: CDAN1

Linked Data

• MyVariant Identifiers: chr15:g.43023524T>G (hg19) ; chr15:g.42731326T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42731326T>G , CM000677.2:g.42731326T>G	GRCh38
NC_000015.9:g.43023524T>G , CM000677.1:g.43023524T>G	GRCh37
NC_000015.8:g.40810816T>G	NCBI36
NG_012491.1:g.10894A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356231.4:c.1745A>C MANE Select	ENSP00000348564.3:p.Gln582Pro
ENST00000643434.1:c.*923A>C	ENSP00000494699.1:n.*923A>C
ENST00000356231.3:c.1745A>C	ENSP00000348564.3:p.Gln582Pro
NM_138477.2:c.1745A>C	NP_612486.2:p.Gln582Pro
XM_005254176.3:c.1748A>C	XP_005254233.1:p.Gln583Pro
XM_011521270.1:c.1772A>C	XP_011519572.1:p.Gln591Pro
XM_011521271.1:c.1769A>C	XP_011519573.1:p.Gln590Pro
XM_011521272.1:c.1772A>C	XP_011519574.1:p.Gln591Pro
XM_011521273.1:c.1772A>C	XP_011519575.1:p.Gln591Pro
XM_011521274.1:c.737A>C	XP_011519576.1:p.Gln246Pro
XM_011521275.1:c.989A>C	XP_011519577.1:p.Gln330Pro
XR_931757.1:n.1783A>C
NM_138477.4:c.1745A>C MANE Select	NP_612486.2:p.Gln582Pro
XM_005254176.5:c.1748A>C	XP_005254233.1:p.Gln583Pro
XM_011521270.2:c.1772A>C	XP_011519572.1:p.Gln591Pro
XM_011521271.2:c.1769A>C	XP_011519573.1:p.Gln590Pro
XM_011521274.2:c.737A>C	XP_011519576.1:p.Gln246Pro
XR_001751104.1:n.1802A>C
XR_001751105.1:n.1802A>C
XR_931757.2:n.1803A>C