Canonical Allele Identifier: CA490001914

Gene: CDAN1

Linked Data

• MyVariant Identifiers: chr15:g.43023484G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42731286G>A , CM000677.2:g.42731286G>A	GRCh38
NC_000015.9:g.43023484G>A , CM000677.1:g.43023484G>A	GRCh37
NC_000015.8:g.40810776G>A	NCBI36
NG_012491.1:g.10934C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000356231.4:c.1785C>T MANE Select	ENSP00000348564.3:p.Ile595=
ENST00000643434.1:c.*963C>T	ENSP00000494699.1:n.*963C>T
ENST00000356231.3:c.1785C>T	ENSP00000348564.3:p.Ile595=
NM_138477.2:c.1785C>T	NP_612486.2:p.Ile595=
XM_005254176.3:c.1788C>T	XP_005254233.1:p.Ile596=
XM_011521270.1:c.1812C>T	XP_011519572.1:p.Ile604=
XM_011521271.1:c.1809C>T	XP_011519573.1:p.Ile603=
XM_011521272.1:c.1812C>T	XP_011519574.1:p.Ile604=
XM_011521273.1:c.1812C>T	XP_011519575.1:p.Ile604=
XM_011521274.1:c.777C>T	XP_011519576.1:p.Ile259=
XM_011521275.1:c.1029C>T	XP_011519577.1:p.Ile343=
XR_931757.1:n.1823C>T
NM_138477.4:c.1785C>T MANE Select	NP_612486.2:p.Ile595=
XM_005254176.5:c.1788C>T	XP_005254233.1:p.Ile596=
XM_011521270.2:c.1812C>T	XP_011519572.1:p.Ile604=
XM_011521271.2:c.1809C>T	XP_011519573.1:p.Ile603=
XM_011521274.2:c.777C>T	XP_011519576.1:p.Ile259=
XR_001751104.1:n.1842C>T
XR_001751105.1:n.1842C>T
XR_931757.2:n.1843C>T