Canonical Allele Identifier: CA2718444

Gene: DCUN1D1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.182963952C>T , CM000665.2:g.182963952C>T	GRCh38
NC_000003.11:g.182681740C>T , CM000665.1:g.182681740C>T	GRCh37
NC_000003.10:g.184164434C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292782.9:c.318G>A MANE Select	ENSP00000292782.4:p.Ala106=
ENST00000460412.6:c.273G>A	ENSP00000419440.2:p.Ala91=
ENST00000292782.8:c.318G>A	ENSP00000292782.4:p.Ala106=
ENST00000460412.5:c.273G>A	ENSP00000419440.1:p.Ala91=
ENST00000469954.5:c.273G>A	ENSP00000419359.1:p.Ala91=
ENST00000487822.5:c.273G>A	ENSP00000418913.1:p.Ala91=
ENST00000492563.1:c.*68G>A	ENSP00000418935.1:n.*68G>A
ENST00000497606.5:c.273G>A	ENSP00000417675.1:p.Ala91=
ENST00000632685.1:c.273G>A	ENSP00000488427.1:p.Ala91=
NM_001308101.1:c.273G>A	NP_001295030.1:p.Ala91=
NM_020640.2:c.318G>A	NP_065691.2:p.Ala106=
NM_020640.3:c.318G>A	NP_065691.2:p.Ala106=
XM_011512912.1:c.318G>A	XP_011511214.1:p.Ala106=
XM_011512913.1:c.318G>A	XP_011511215.1:p.Ala106=
XM_011512914.1:c.273G>A	XP_011511216.1:p.Ala91=
XM_011512915.1:c.273G>A	XP_011511217.1:p.Ala91=
XM_011512916.1:c.273G>A	XP_011511218.1:p.Ala91=
XM_011512912.2:c.318G>A	XP_011511214.1:p.Ala106=
XM_011512915.2:c.273G>A	XP_011511217.1:p.Ala91=
XM_011512916.2:c.273G>A	XP_011511218.1:p.Ala91=
XM_017006633.1:c.273G>A	XP_016862122.1:p.Ala91=
XM_017006634.1:c.273G>A	XP_016862123.1:p.Ala91=
XM_017006635.2:c.273G>A	XP_016862124.1:p.Ala91=
XM_024453601.1:c.273G>A	XP_024309369.1:p.Ala91=
NM_001308101.2:c.273G>A	NP_001295030.1:p.Ala91=
NM_020640.4:c.318G>A MANE Select	NP_065691.2:p.Ala106=