Canonical Allele Identifier: CA490002038

Gene: CDAN1

Linked Data

• MyVariant Identifiers: chr15:g.43023424T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42731226T>A , CM000677.2:g.42731226T>A	GRCh38
NC_000015.9:g.43023424T>A , CM000677.1:g.43023424T>A	GRCh37
NC_000015.8:g.40810716T>A	NCBI36
NG_012491.1:g.10994A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356231.4:c.1845A>T MANE Select	ENSP00000348564.3:p.Ser615=
ENST00000643434.1:c.*1023A>T	ENSP00000494699.1:n.*1023A>T
ENST00000356231.3:c.1845A>T	ENSP00000348564.3:p.Ser615=
NM_138477.2:c.1845A>T	NP_612486.2:p.Ser615=
XM_005254176.3:c.1848A>T	XP_005254233.1:p.Ser616=
XM_011521270.1:c.1872A>T	XP_011519572.1:p.Ser624=
XM_011521271.1:c.1869A>T	XP_011519573.1:p.Ser623=
XM_011521272.1:c.1872A>T	XP_011519574.1:p.Ser624=
XM_011521273.1:c.1872A>T	XP_011519575.1:p.Ser624=
XM_011521274.1:c.837A>T	XP_011519576.1:p.Ser279=
XM_011521275.1:c.1089A>T	XP_011519577.1:p.Ser363=
XR_931757.1:n.1883A>T
NM_138477.4:c.1845A>T MANE Select	NP_612486.2:p.Ser615=
XM_005254176.5:c.1848A>T	XP_005254233.1:p.Ser616=
XM_011521270.2:c.1872A>T	XP_011519572.1:p.Ser624=
XM_011521271.2:c.1869A>T	XP_011519573.1:p.Ser623=
XM_011521274.2:c.837A>T	XP_011519576.1:p.Ser279=
XR_001751104.1:n.1902A>T
XR_001751105.1:n.1902A>T
XR_931757.2:n.1903A>T