Canonical Allele Identifier: CA2172870521

Gene: CDAN1

Linked Data

• dbSNP Id: rs2061611143
• gnomAD v4: 15-42731499-AAGTTGGAGCTGGAAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42731500_42731514del , CM000677.2:g.42731500_42731514del	GRCh38
NC_000015.9:g.43023698_43023712del , CM000677.1:g.43023698_43023712del	GRCh37
NC_000015.8:g.40810990_40811004del	NCBI36
NG_012491.1:g.10706_10720del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356231.4:c.1739+106_1739+120del MANE Select	ENSP00000348564.3:n.1739+106_1739+120del
ENST00000643434.1:c.*917+106_*917+120del	ENSP00000494699.1:n.*917+106_*917+120del
ENST00000356231.3:c.1739+106_1739+120del	ENSP00000348564.3:n.1739+106_1739+120del
NM_138477.2:c.1739+106_1739+120del	NP_612486.2:n.1739+106_1739+120del
XM_005254176.3:c.1742+106_1742+120del	XP_005254233.1:n.1742+106_1742+120del
XM_011521270.1:c.1766+106_1766+120del	XP_011519572.1:n.1766+106_1766+120del
XM_011521271.1:c.1763+106_1763+120del	XP_011519573.1:n.1763+106_1763+120del
XM_011521272.1:c.1766+106_1766+120del	XP_011519574.1:n.1766+106_1766+120del
XM_011521273.1:c.1766+106_1766+120del	XP_011519575.1:n.1766+106_1766+120del
XM_011521274.1:c.731+106_731+120del	XP_011519576.1:n.731+106_731+120del
XM_011521275.1:c.983+106_983+120del	XP_011519577.1:n.983+106_983+120del
XR_931757.1:n.1777+106_1777+120del
NM_138477.4:c.1739+106_1739+120del MANE Select	NP_612486.2:n.1739+106_1739+120del
XM_005254176.5:c.1742+106_1742+120del	XP_005254233.1:n.1742+106_1742+120del
XM_011521270.2:c.1766+106_1766+120del	XP_011519572.1:n.1766+106_1766+120del
XM_011521271.2:c.1763+106_1763+120del	XP_011519573.1:n.1763+106_1763+120del
XM_011521274.2:c.731+106_731+120del	XP_011519576.1:n.731+106_731+120del
XR_001751104.1:n.1796+106_1796+120del
XR_001751105.1:n.1796+106_1796+120del
XR_931757.2:n.1797+106_1797+120del