Canonical Allele Identifier: CA2628074024

Gene: CDAN1

Linked Data

• gnomAD v4: 15-42731528-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42731528G>T , CM000677.2:g.42731528G>T	GRCh38
NC_000015.9:g.43023726G>T , CM000677.1:g.43023726G>T	GRCh37
NC_000015.8:g.40811018G>T	NCBI36
NG_012491.1:g.10692C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356231.4:c.1739+92C>A MANE Select	ENSP00000348564.3:n.1739+92C>A
ENST00000643434.1:c.*917+92C>A	ENSP00000494699.1:n.*917+92C>A
ENST00000356231.3:c.1739+92C>A	ENSP00000348564.3:n.1739+92C>A
NM_138477.2:c.1739+92C>A	NP_612486.2:n.1739+92C>A
XM_005254176.3:c.1742+92C>A	XP_005254233.1:n.1742+92C>A
XM_011521270.1:c.1766+92C>A	XP_011519572.1:n.1766+92C>A
XM_011521271.1:c.1763+92C>A	XP_011519573.1:n.1763+92C>A
XM_011521272.1:c.1766+92C>A	XP_011519574.1:n.1766+92C>A
XM_011521273.1:c.1766+92C>A	XP_011519575.1:n.1766+92C>A
XM_011521274.1:c.731+92C>A	XP_011519576.1:n.731+92C>A
XM_011521275.1:c.983+92C>A	XP_011519577.1:n.983+92C>A
XR_931757.1:n.1777+92C>A
NM_138477.4:c.1739+92C>A MANE Select	NP_612486.2:n.1739+92C>A
XM_005254176.5:c.1742+92C>A	XP_005254233.1:n.1742+92C>A
XM_011521270.2:c.1766+92C>A	XP_011519572.1:n.1766+92C>A
XM_011521271.2:c.1763+92C>A	XP_011519573.1:n.1763+92C>A
XM_011521274.2:c.731+92C>A	XP_011519576.1:n.731+92C>A
XR_001751104.1:n.1796+92C>A
XR_001751105.1:n.1796+92C>A
XR_931757.2:n.1797+92C>A