Canonical Allele Identifier: CA392044954

Gene: CDAN1

Linked Data

• MyVariant Identifiers: chr15:g.43023481C>A (hg19) ; chr15:g.42731283C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42731283C>A , CM000677.2:g.42731283C>A	GRCh38
NC_000015.9:g.43023481C>A , CM000677.1:g.43023481C>A	GRCh37
NC_000015.8:g.40810773C>A	NCBI36
NG_012491.1:g.10937G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356231.4:c.1788G>T MANE Select	ENSP00000348564.3:p.Gln596His
ENST00000643434.1:c.*966G>T	ENSP00000494699.1:n.*966G>T
ENST00000356231.3:c.1788G>T	ENSP00000348564.3:p.Gln596His
NM_138477.2:c.1788G>T	NP_612486.2:p.Gln596His
XM_005254176.3:c.1791G>T	XP_005254233.1:p.Gln597His
XM_011521270.1:c.1815G>T	XP_011519572.1:p.Gln605His
XM_011521271.1:c.1812G>T	XP_011519573.1:p.Gln604His
XM_011521272.1:c.1815G>T	XP_011519574.1:p.Gln605His
XM_011521273.1:c.1815G>T	XP_011519575.1:p.Gln605His
XM_011521274.1:c.780G>T	XP_011519576.1:p.Gln260His
XM_011521275.1:c.1032G>T	XP_011519577.1:p.Gln344His
XR_931757.1:n.1826G>T
NM_138477.4:c.1788G>T MANE Select	NP_612486.2:p.Gln596His
XM_005254176.5:c.1791G>T	XP_005254233.1:p.Gln597His
XM_011521270.2:c.1815G>T	XP_011519572.1:p.Gln605His
XM_011521271.2:c.1812G>T	XP_011519573.1:p.Gln604His
XM_011521274.2:c.780G>T	XP_011519576.1:p.Gln260His
XR_001751104.1:n.1845G>T
XR_001751105.1:n.1845G>T
XR_931757.2:n.1846G>T