Canonical Allele Identifier: CA392045242

Gene: CDAN1

Linked Data

• MyVariant Identifiers: chr15:g.43023525G>C (hg19) ; chr15:g.42731327G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42731327G>C , CM000677.2:g.42731327G>C	GRCh38
NC_000015.9:g.43023525G>C , CM000677.1:g.43023525G>C	GRCh37
NC_000015.8:g.40810817G>C	NCBI36
NG_012491.1:g.10893C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356231.4:c.1744C>G MANE Select	ENSP00000348564.3:p.Gln582Glu
ENST00000643434.1:c.*922C>G	ENSP00000494699.1:n.*922C>G
ENST00000356231.3:c.1744C>G	ENSP00000348564.3:p.Gln582Glu
NM_138477.2:c.1744C>G	NP_612486.2:p.Gln582Glu
XM_005254176.3:c.1747C>G	XP_005254233.1:p.Gln583Glu
XM_011521270.1:c.1771C>G	XP_011519572.1:p.Gln591Glu
XM_011521271.1:c.1768C>G	XP_011519573.1:p.Gln590Glu
XM_011521272.1:c.1771C>G	XP_011519574.1:p.Gln591Glu
XM_011521273.1:c.1771C>G	XP_011519575.1:p.Gln591Glu
XM_011521274.1:c.736C>G	XP_011519576.1:p.Gln246Glu
XM_011521275.1:c.988C>G	XP_011519577.1:p.Gln330Glu
XR_931757.1:n.1782C>G
NM_138477.4:c.1744C>G MANE Select	NP_612486.2:p.Gln582Glu
XM_005254176.5:c.1747C>G	XP_005254233.1:p.Gln583Glu
XM_011521270.2:c.1771C>G	XP_011519572.1:p.Gln591Glu
XM_011521271.2:c.1768C>G	XP_011519573.1:p.Gln590Glu
XM_011521274.2:c.736C>G	XP_011519576.1:p.Gln246Glu
XR_001751104.1:n.1801C>G
XR_001751105.1:n.1801C>G
XR_931757.2:n.1802C>G