Canonical Allele Identifier: CA392045176

Gene: CDAN1

Linked Data

• gnomAD v4: 15-42731317-T-C
• MyVariant Identifiers: chr15:g.43023515T>C (hg19) ; chr15:g.42731317T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42731317T>C , CM000677.2:g.42731317T>C	GRCh38
NC_000015.9:g.43023515T>C , CM000677.1:g.43023515T>C	GRCh37
NC_000015.8:g.40810807T>C	NCBI36
NG_012491.1:g.10903A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356231.4:c.1754A>G MANE Select	ENSP00000348564.3:p.Gln585Arg
ENST00000643434.1:c.*932A>G	ENSP00000494699.1:n.*932A>G
ENST00000356231.3:c.1754A>G	ENSP00000348564.3:p.Gln585Arg
NM_138477.2:c.1754A>G	NP_612486.2:p.Gln585Arg
XM_005254176.3:c.1757A>G	XP_005254233.1:p.Gln586Arg
XM_011521270.1:c.1781A>G	XP_011519572.1:p.Gln594Arg
XM_011521271.1:c.1778A>G	XP_011519573.1:p.Gln593Arg
XM_011521272.1:c.1781A>G	XP_011519574.1:p.Gln594Arg
XM_011521273.1:c.1781A>G	XP_011519575.1:p.Gln594Arg
XM_011521274.1:c.746A>G	XP_011519576.1:p.Gln249Arg
XM_011521275.1:c.998A>G	XP_011519577.1:p.Gln333Arg
XR_931757.1:n.1792A>G
NM_138477.4:c.1754A>G MANE Select	NP_612486.2:p.Gln585Arg
XM_005254176.5:c.1757A>G	XP_005254233.1:p.Gln586Arg
XM_011521270.2:c.1781A>G	XP_011519572.1:p.Gln594Arg
XM_011521271.2:c.1778A>G	XP_011519573.1:p.Gln593Arg
XM_011521274.2:c.746A>G	XP_011519576.1:p.Gln249Arg
XR_001751104.1:n.1811A>G
XR_001751105.1:n.1811A>G
XR_931757.2:n.1812A>G