Canonical Allele Identifier: CA7515553

Gene: CDAN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42729063C>T , CM000677.2:g.42729063C>T	GRCh38
NC_000015.9:g.43021261C>T , CM000677.1:g.43021261C>T	GRCh37
NC_000015.8:g.40808553C>T	NCBI36
NG_012491.1:g.13157G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356231.4:c.2605G>A MANE Select	ENSP00000348564.3:p.Val869Met
ENST00000643434.1:c.*1783G>A	ENSP00000494699.1:n.*1783G>A
ENST00000356231.3:c.2605G>A	ENSP00000348564.3:p.Val869Met
ENST00000562465.5:c.598G>A	ENSP00000454246.1:p.Val200Met
NM_138477.2:c.2605G>A	NP_612486.2:p.Val869Met
XM_005254176.3:c.2608G>A	XP_005254233.1:p.Val870Met
XM_011521270.1:c.2632G>A	XP_011519572.1:p.Val878Met
XM_011521271.1:c.2629G>A	XP_011519573.1:p.Val877Met
XM_011521272.1:c.2632G>A	XP_011519574.1:p.Val878Met
XM_011521273.1:c.2632G>A	XP_011519575.1:p.Val878Met
XM_011521274.1:c.1597G>A	XP_011519576.1:p.Val533Met
XM_011521275.1:c.1849G>A	XP_011519577.1:p.Val617Met
NM_138477.4:c.2605G>A MANE Select	NP_612486.2:p.Val869Met
XM_005254176.5:c.2608G>A	XP_005254233.1:p.Val870Met
XM_011521270.2:c.2632G>A	XP_011519572.1:p.Val878Met
XM_011521271.2:c.2629G>A	XP_011519573.1:p.Val877Met
XM_011521274.2:c.1597G>A	XP_011519576.1:p.Val533Met
XR_001751104.1:n.2662G>A
XR_001751105.1:n.2662G>A