Canonical Allele Identifier: CA2172870414

Gene: CDAN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42731285G= , CM000677.2:g.42731285G=	GRCh38
NC_000015.9:g.43023483G= , CM000677.1:g.43023483G=	GRCh37
NC_000015.8:g.40810775G=	NCBI36
NG_012491.1:g.10935C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000356231.4:c.1786C= MANE Select	ENSP00000348564.3:p.Gln596=
ENST00000643434.1:c.*964C=	ENSP00000494699.1:n.*964C=
ENST00000356231.3:c.1786C=	ENSP00000348564.3:p.Gln596=
NM_138477.2:c.1786C=	NP_612486.2:p.Gln596=
XM_005254176.3:c.1789C=	XP_005254233.1:p.Gln597=
XM_011521270.1:c.1813C=	XP_011519572.1:p.Gln605=
XM_011521271.1:c.1810C=	XP_011519573.1:p.Gln604=
XM_011521272.1:c.1813C=	XP_011519574.1:p.Gln605=
XM_011521273.1:c.1813C=	XP_011519575.1:p.Gln605=
XM_011521274.1:c.778C=	XP_011519576.1:p.Gln260=
XM_011521275.1:c.1030C=	XP_011519577.1:p.Gln344=
XR_931757.1:n.1824C=
NM_138477.4:c.1786C= MANE Select	NP_612486.2:p.Gln596=
XM_005254176.5:c.1789C=	XP_005254233.1:p.Gln597=
XM_011521270.2:c.1813C=	XP_011519572.1:p.Gln605=
XM_011521271.2:c.1810C=	XP_011519573.1:p.Gln604=
XM_011521274.2:c.778C=	XP_011519576.1:p.Gln260=
XR_001751104.1:n.1843C=
XR_001751105.1:n.1843C=
XR_931757.2:n.1844C=