Canonical Allele Identifier: CA7516416

Gene: CDAN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42736428G>A , CM000677.2:g.42736428G>A	GRCh38
NC_000015.9:g.43028626G>A , CM000677.1:g.43028626G>A	GRCh37
NC_000015.8:g.40815918G>A	NCBI36
NG_012491.1:g.5792C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356231.4:c.443C>T MANE Select	ENSP00000348564.3:p.Ala148Val
ENST00000643434.1:c.91-347C>T	ENSP00000494699.1:n.91-347C>T
ENST00000356231.3:c.443C>T	ENSP00000348564.3:p.Ala148Val
NM_138477.2:c.443C>T	NP_612486.2:p.Ala148Val
XM_005254176.3:c.443C>T	XP_005254233.1:p.Ala148Val
XM_011521270.1:c.467C>T	XP_011519572.1:p.Ala156Val
XM_011521271.1:c.467C>T	XP_011519573.1:p.Ala156Val
XM_011521272.1:c.467C>T	XP_011519574.1:p.Ala156Val
XM_011521273.1:c.467C>T	XP_011519575.1:p.Ala156Val
XM_011521275.1:c.-190-347C>T	XP_011519577.1:n.-190-347C>T
XR_931757.1:n.478C>T
NM_138477.4:c.443C>T MANE Select	NP_612486.2:p.Ala148Val
XM_005254176.5:c.443C>T	XP_005254233.1:p.Ala148Val
XM_011521270.2:c.467C>T	XP_011519572.1:p.Ala156Val
XM_011521271.2:c.467C>T	XP_011519573.1:p.Ala156Val
XR_001751104.1:n.497C>T
XR_001751105.1:n.497C>T
XR_931757.2:n.498C>T