Canonical Allele Identifier: CA392060811

Gene: CDAN1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42736715G>T , CM000677.2:g.42736715G>T	GRCh38
NC_000015.9:g.43028913G>T , CM000677.1:g.43028913G>T	GRCh37
NC_000015.8:g.40816205G>T	NCBI36
NG_012491.1:g.5505C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356231.4:c.156C>A MANE Select	ENSP00000348564.3:p.Phe52Leu
ENST00000643434.1:c.90+298C>A	ENSP00000494699.1:n.90+298C>A
ENST00000356231.3:c.156C>A	ENSP00000348564.3:p.Phe52Leu
ENST00000563260.1:c.132C>A	ENSP00000455536.1:p.Phe44Leu
NM_138477.2:c.156C>A	NP_612486.2:p.Phe52Leu
XM_005254176.3:c.156C>A	XP_005254233.1:p.Phe52Leu
XM_011521270.1:c.180C>A	XP_011519572.1:p.Phe60Leu
XM_011521271.1:c.180C>A	XP_011519573.1:p.Phe60Leu
XM_011521272.1:c.180C>A	XP_011519574.1:p.Phe60Leu
XM_011521273.1:c.180C>A	XP_011519575.1:p.Phe60Leu
XM_011521275.1:c.-191+298C>A	XP_011519577.1:n.-191+298C>A
XR_931757.1:n.191C>A
NM_138477.4:c.156C>A MANE Select	NP_612486.2:p.Phe52Leu
XM_005254176.5:c.156C>A	XP_005254233.1:p.Phe52Leu
XM_011521270.2:c.180C>A	XP_011519572.1:p.Phe60Leu
XM_011521271.2:c.180C>A	XP_011519573.1:p.Phe60Leu
XR_001751104.1:n.210C>A
XR_001751105.1:n.210C>A
XR_931757.2:n.211C>A