Canonical Allele Identifier: CA7515570

Gene: CDAN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42729091C>T , CM000677.2:g.42729091C>T	GRCh38
NC_000015.9:g.43021289C>T , CM000677.1:g.43021289C>T	GRCh37
NC_000015.8:g.40808581C>T	NCBI36
NG_012491.1:g.13129G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356231.4:c.2577G>A MANE Select	ENSP00000348564.3:p.Pro859=
ENST00000643434.1:c.*1755G>A	ENSP00000494699.1:n.*1755G>A
ENST00000356231.3:c.2577G>A	ENSP00000348564.3:p.Pro859=
ENST00000562465.5:c.570G>A	ENSP00000454246.1:p.Pro190=
NM_138477.2:c.2577G>A	NP_612486.2:p.Pro859=
XM_005254176.3:c.2580G>A	XP_005254233.1:p.Pro860=
XM_011521270.1:c.2604G>A	XP_011519572.1:p.Pro868=
XM_011521271.1:c.2601G>A	XP_011519573.1:p.Pro867=
XM_011521272.1:c.2604G>A	XP_011519574.1:p.Pro868=
XM_011521273.1:c.2604G>A	XP_011519575.1:p.Pro868=
XM_011521274.1:c.1569G>A	XP_011519576.1:p.Pro523=
XM_011521275.1:c.1821G>A	XP_011519577.1:p.Pro607=
NM_138477.4:c.2577G>A MANE Select	NP_612486.2:p.Pro859=
XM_005254176.5:c.2580G>A	XP_005254233.1:p.Pro860=
XM_011521270.2:c.2604G>A	XP_011519572.1:p.Pro868=
XM_011521271.2:c.2601G>A	XP_011519573.1:p.Pro867=
XM_011521274.2:c.1569G>A	XP_011519576.1:p.Pro523=
XR_001751104.1:n.2634G>A
XR_001751105.1:n.2634G>A