Canonical Allele Identifier: CA489895216

Gene: CDAN1

Linked Data

• MyVariant Identifiers: chr15:g.43022861A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42730663A>T , CM000677.2:g.42730663A>T	GRCh38
NC_000015.9:g.43022861A>T , CM000677.1:g.43022861A>T	GRCh37
NC_000015.8:g.40810153A>T	NCBI36
NG_012491.1:g.11557T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000356231.4:c.2109T>A MANE Select	ENSP00000348564.3:p.Ala703=
ENST00000643434.1:c.*1287T>A	ENSP00000494699.1:n.*1287T>A
ENST00000356231.3:c.2109T>A	ENSP00000348564.3:p.Ala703=
ENST00000562465.5:c.102T>A	ENSP00000454246.1:p.Ala34=
NM_138477.2:c.2109T>A	NP_612486.2:p.Ala703=
XM_005254176.3:c.2112T>A	XP_005254233.1:p.Ala704=
XM_011521270.1:c.2136T>A	XP_011519572.1:p.Ala712=
XM_011521271.1:c.2133T>A	XP_011519573.1:p.Ala711=
XM_011521272.1:c.2136T>A	XP_011519574.1:p.Ala712=
XM_011521273.1:c.2136T>A	XP_011519575.1:p.Ala712=
XM_011521274.1:c.1101T>A	XP_011519576.1:p.Ala367=
XM_011521275.1:c.1353T>A	XP_011519577.1:p.Ala451=
XR_931757.1:n.2109T>A
NM_138477.4:c.2109T>A MANE Select	NP_612486.2:p.Ala703=
XM_005254176.5:c.2112T>A	XP_005254233.1:p.Ala704=
XM_011521270.2:c.2136T>A	XP_011519572.1:p.Ala712=
XM_011521271.2:c.2133T>A	XP_011519573.1:p.Ala711=
XM_011521274.2:c.1101T>A	XP_011519576.1:p.Ala367=
XR_001751104.1:n.2166T>A
XR_001751105.1:n.2166T>A
XR_931757.2:n.2129T>A