Canonical Allele Identifier: CA2172870520

Gene: CDAN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42731499_42731514delinsAAGTTGGAGCTGGAAG , CM000677.2:g.42731499_42731514delinsAAGTTGGAGCTGGAAG	GRCh38
NC_000015.9:g.43023697_43023712delinsAAGTTGGAGCTGGAAG , CM000677.1:g.43023697_43023712delinsAAGTTGGAGCTGGAAG	GRCh37
NC_000015.8:g.40810989_40811004delinsAAGTTGGAGCTGGAAG	NCBI36
NG_012491.1:g.10706_10721delinsCTTCCAGCTCCAACTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356231.4:c.1739+106_1739+121delinsCTTCCAGCTCCAACTT MANE Select	ENSP00000348564.3:n.1739+106_1739+121delinsCTTCCAGCTCCAACTT
ENST00000643434.1:c.*917+106_*917+121delinsCTTCCAGCTCCAACTT	ENSP00000494699.1:n.*917+106_*917+121delinsCTTCCAGCTCCAACTT
ENST00000356231.3:c.1739+106_1739+121delinsCTTCCAGCTCCAACTT	ENSP00000348564.3:n.1739+106_1739+121delinsCTTCCAGCTCCAACTT
NM_138477.2:c.1739+106_1739+121delinsCTTCCAGCTCCAACTT	NP_612486.2:n.1739+106_1739+121delinsCTTCCAGCTCCAACTT
XM_005254176.3:c.1742+106_1742+121delinsCTTCCAGCTCCAACTT	XP_005254233.1:n.1742+106_1742+121delinsCTTCCAGCTCCAACTT
XM_011521270.1:c.1766+106_1766+121delinsCTTCCAGCTCCAACTT	XP_011519572.1:n.1766+106_1766+121delinsCTTCCAGCTCCAACTT
XM_011521271.1:c.1763+106_1763+121delinsCTTCCAGCTCCAACTT	XP_011519573.1:n.1763+106_1763+121delinsCTTCCAGCTCCAACTT
XM_011521272.1:c.1766+106_1766+121delinsCTTCCAGCTCCAACTT	XP_011519574.1:n.1766+106_1766+121delinsCTTCCAGCTCCAACTT
XM_011521273.1:c.1766+106_1766+121delinsCTTCCAGCTCCAACTT	XP_011519575.1:n.1766+106_1766+121delinsCTTCCAGCTCCAACTT
XM_011521274.1:c.731+106_731+121delinsCTTCCAGCTCCAACTT	XP_011519576.1:n.731+106_731+121delinsCTTCCAGCTCCAACTT
XM_011521275.1:c.983+106_983+121delinsCTTCCAGCTCCAACTT	XP_011519577.1:n.983+106_983+121delinsCTTCCAGCTCCAACTT
XR_931757.1:n.1777+106_1777+121delinsCTTCCAGCTCCAACTT
NM_138477.4:c.1739+106_1739+121delinsCTTCCAGCTCCAACTT MANE Select	NP_612486.2:n.1739+106_1739+121delinsCTTCCAGCTCCAACTT
XM_005254176.5:c.1742+106_1742+121delinsCTTCCAGCTCCAACTT	XP_005254233.1:n.1742+106_1742+121delinsCTTCCAGCTCCAACTT
XM_011521270.2:c.1766+106_1766+121delinsCTTCCAGCTCCAACTT	XP_011519572.1:n.1766+106_1766+121delinsCTTCCAGCTCCAACTT
XM_011521271.2:c.1763+106_1763+121delinsCTTCCAGCTCCAACTT	XP_011519573.1:n.1763+106_1763+121delinsCTTCCAGCTCCAACTT
XM_011521274.2:c.731+106_731+121delinsCTTCCAGCTCCAACTT	XP_011519576.1:n.731+106_731+121delinsCTTCCAGCTCCAACTT
XR_001751104.1:n.1796+106_1796+121delinsCTTCCAGCTCCAACTT
XR_001751105.1:n.1796+106_1796+121delinsCTTCCAGCTCCAACTT
XR_931757.2:n.1797+106_1797+121delinsCTTCCAGCTCCAACTT