Canonical Allele Identifier: CA7515160

Gene: CDAN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42725555C>T , CM000677.2:g.42725555C>T	GRCh38
NC_000015.9:g.43017753C>T , CM000677.1:g.43017753C>T	GRCh37
NC_000015.8:g.40805045C>T	NCBI36
NG_012491.1:g.16665G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356231.4:c.3384G>A MANE Select	ENSP00000348564.3:p.Pro1128=
ENST00000643434.1:c.*2451G>A	ENSP00000494699.1:n.*2451G>A
ENST00000356231.3:c.3384G>A	ENSP00000348564.3:p.Pro1128=
ENST00000562465.5:c.1330G>A	ENSP00000454246.1:n.1330G>A
ENST00000563604.1:n.83G>A
NM_138477.2:c.3384G>A	NP_612486.2:p.Pro1128=
XM_005254176.3:c.3387G>A	XP_005254233.1:p.Pro1129=
XM_011521270.1:c.3411G>A	XP_011519572.1:p.Pro1137=
XM_011521271.1:c.3408G>A	XP_011519573.1:p.Pro1136=
XM_011521274.1:c.2376G>A	XP_011519576.1:p.Pro792=
XM_011521275.1:c.2628G>A	XP_011519577.1:p.Pro876=
NM_138477.4:c.3384G>A MANE Select	NP_612486.2:p.Pro1128=
XM_005254176.5:c.3387G>A	XP_005254233.1:p.Pro1129=
XM_011521270.2:c.3411G>A	XP_011519572.1:p.Pro1137=
XM_011521271.2:c.3408G>A	XP_011519573.1:p.Pro1136=
XM_011521274.2:c.2376G>A	XP_011519576.1:p.Pro792=
XR_001751104.1:n.3377G>A
XR_001751105.1:n.3394G>A