Canonical Allele Identifier: CA7515265

Gene: CDAN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42726372C>T , CM000677.2:g.42726372C>T	GRCh38
NC_000015.9:g.43018570C>T , CM000677.1:g.43018570C>T	GRCh37
NC_000015.8:g.40805862C>T	NCBI36
NG_012491.1:g.15848G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356231.4:c.3142G>A MANE Select	ENSP00000348564.3:p.Val1048Ile
ENST00000643434.1:c.*2273G>A	ENSP00000494699.1:n.*2273G>A
ENST00000356231.3:c.3142G>A	ENSP00000348564.3:p.Val1048Ile
ENST00000562465.5:c.1088G>A	ENSP00000454246.1:n.1088G>A
NM_138477.2:c.3142G>A	NP_612486.2:p.Val1048Ile
XM_005254176.3:c.3145G>A	XP_005254233.1:p.Val1049Ile
XM_011521270.1:c.3169G>A	XP_011519572.1:p.Val1057Ile
XM_011521271.1:c.3166G>A	XP_011519573.1:p.Val1056Ile
XM_011521272.1:c.3169G>A	XP_011519574.1:p.Val1057Ile
XM_011521273.1:c.*44G>A	XP_011519575.1:n.*44G>A
XM_011521274.1:c.2134G>A	XP_011519576.1:p.Val712Ile
XM_011521275.1:c.2386G>A	XP_011519577.1:p.Val796Ile
NM_138477.4:c.3142G>A MANE Select	NP_612486.2:p.Val1048Ile
XM_005254176.5:c.3145G>A	XP_005254233.1:p.Val1049Ile
XM_011521270.2:c.3169G>A	XP_011519572.1:p.Val1057Ile
XM_011521271.2:c.3166G>A	XP_011519573.1:p.Val1056Ile
XM_011521274.2:c.2134G>A	XP_011519576.1:p.Val712Ile
XR_001751104.1:n.3199G>A
XR_001751105.1:n.3152G>A