Canonical Allele Identifier: CA489895200

Gene: CDAN1

Linked Data

• MyVariant Identifiers: chr15:g.43022840C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42730642C>A , CM000677.2:g.42730642C>A	GRCh38
NC_000015.9:g.43022840C>A , CM000677.1:g.43022840C>A	GRCh37
NC_000015.8:g.40810132C>A	NCBI36
NG_012491.1:g.11578G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000356231.4:c.2130G>T MANE Select	ENSP00000348564.3:p.Leu710=
ENST00000643434.1:c.*1308G>T	ENSP00000494699.1:n.*1308G>T
ENST00000356231.3:c.2130G>T	ENSP00000348564.3:p.Leu710=
ENST00000562465.5:c.123G>T	ENSP00000454246.1:p.Leu41=
NM_138477.2:c.2130G>T	NP_612486.2:p.Leu710=
XM_005254176.3:c.2133G>T	XP_005254233.1:p.Leu711=
XM_011521270.1:c.2157G>T	XP_011519572.1:p.Leu719=
XM_011521271.1:c.2154G>T	XP_011519573.1:p.Leu718=
XM_011521272.1:c.2157G>T	XP_011519574.1:p.Leu719=
XM_011521273.1:c.2157G>T	XP_011519575.1:p.Leu719=
XM_011521274.1:c.1122G>T	XP_011519576.1:p.Leu374=
XM_011521275.1:c.1374G>T	XP_011519577.1:p.Leu458=
XR_931757.1:n.2130G>T
NM_138477.4:c.2130G>T MANE Select	NP_612486.2:p.Leu710=
XM_005254176.5:c.2133G>T	XP_005254233.1:p.Leu711=
XM_011521270.2:c.2157G>T	XP_011519572.1:p.Leu719=
XM_011521271.2:c.2154G>T	XP_011519573.1:p.Leu718=
XM_011521274.2:c.1122G>T	XP_011519576.1:p.Leu374=
XR_001751104.1:n.2187G>T
XR_001751105.1:n.2187G>T
XR_931757.2:n.2150G>T