Canonical Allele Identifier: CA392045106

Gene: CDAN1

Linked Data

• MyVariant Identifiers: chr15:g.43023504C>G (hg19) ; chr15:g.42731306C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42731306C>G , CM000677.2:g.42731306C>G	GRCh38
NC_000015.9:g.43023504C>G , CM000677.1:g.43023504C>G	GRCh37
NC_000015.8:g.40810796C>G	NCBI36
NG_012491.1:g.10914G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356231.4:c.1765G>C MANE Select	ENSP00000348564.3:p.Asp589His
ENST00000643434.1:c.*943G>C	ENSP00000494699.1:n.*943G>C
ENST00000356231.3:c.1765G>C	ENSP00000348564.3:p.Asp589His
NM_138477.2:c.1765G>C	NP_612486.2:p.Asp589His
XM_005254176.3:c.1768G>C	XP_005254233.1:p.Asp590His
XM_011521270.1:c.1792G>C	XP_011519572.1:p.Asp598His
XM_011521271.1:c.1789G>C	XP_011519573.1:p.Asp597His
XM_011521272.1:c.1792G>C	XP_011519574.1:p.Asp598His
XM_011521273.1:c.1792G>C	XP_011519575.1:p.Asp598His
XM_011521274.1:c.757G>C	XP_011519576.1:p.Asp253His
XM_011521275.1:c.1009G>C	XP_011519577.1:p.Asp337His
XR_931757.1:n.1803G>C
NM_138477.4:c.1765G>C MANE Select	NP_612486.2:p.Asp589His
XM_005254176.5:c.1768G>C	XP_005254233.1:p.Asp590His
XM_011521270.2:c.1792G>C	XP_011519572.1:p.Asp598His
XM_011521271.2:c.1789G>C	XP_011519573.1:p.Asp597His
XM_011521274.2:c.757G>C	XP_011519576.1:p.Asp253His
XR_001751104.1:n.1822G>C
XR_001751105.1:n.1822G>C
XR_931757.2:n.1823G>C