Canonical Allele Identifier: CA2172870528

Gene: CDAN1

Linked Data

• dbSNP Id: rs2061611328
• gnomAD v4: 15-42731518-C-CCTATCTCCAGGCAAAGGAGA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42731521_42731540dup , CM000677.2:g.42731521_42731540dup	GRCh38
NC_000015.9:g.43023719_43023738dup , CM000677.1:g.43023719_43023738dup	GRCh37
NC_000015.8:g.40811011_40811030dup	NCBI36
NG_012491.1:g.10682_10701dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356231.4:c.1739+82_1739+101dup MANE Select	ENSP00000348564.3:n.1739+82_1739+101dup
ENST00000643434.1:c.*917+82_*917+101dup	ENSP00000494699.1:n.*917+82_*917+101dup
ENST00000356231.3:c.1739+82_1739+101dup	ENSP00000348564.3:n.1739+82_1739+101dup
NM_138477.2:c.1739+82_1739+101dup	NP_612486.2:n.1739+82_1739+101dup
XM_005254176.3:c.1742+82_1742+101dup	XP_005254233.1:n.1742+82_1742+101dup
XM_011521270.1:c.1766+82_1766+101dup	XP_011519572.1:n.1766+82_1766+101dup
XM_011521271.1:c.1763+82_1763+101dup	XP_011519573.1:n.1763+82_1763+101dup
XM_011521272.1:c.1766+82_1766+101dup	XP_011519574.1:n.1766+82_1766+101dup
XM_011521273.1:c.1766+82_1766+101dup	XP_011519575.1:n.1766+82_1766+101dup
XM_011521274.1:c.731+82_731+101dup	XP_011519576.1:n.731+82_731+101dup
XM_011521275.1:c.983+82_983+101dup	XP_011519577.1:n.983+82_983+101dup
XR_931757.1:n.1777+82_1777+101dup
NM_138477.4:c.1739+82_1739+101dup MANE Select	NP_612486.2:n.1739+82_1739+101dup
XM_005254176.5:c.1742+82_1742+101dup	XP_005254233.1:n.1742+82_1742+101dup
XM_011521270.2:c.1766+82_1766+101dup	XP_011519572.1:n.1766+82_1766+101dup
XM_011521271.2:c.1763+82_1763+101dup	XP_011519573.1:n.1763+82_1763+101dup
XM_011521274.2:c.731+82_731+101dup	XP_011519576.1:n.731+82_731+101dup
XR_001751104.1:n.1796+82_1796+101dup
XR_001751105.1:n.1796+82_1796+101dup
XR_931757.2:n.1797+82_1797+101dup