Canonical Allele Identifier: CA392042185

Gene: CDAN1

Linked Data

• MyVariant Identifiers: chr15:g.43022836A>G (hg19) ; chr15:g.42730638A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42730638A>G , CM000677.2:g.42730638A>G	GRCh38
NC_000015.9:g.43022836A>G , CM000677.1:g.43022836A>G	GRCh37
NC_000015.8:g.40810128A>G	NCBI36
NG_012491.1:g.11582T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000356231.4:c.2134T>C MANE Select	ENSP00000348564.3:p.Tyr712His
ENST00000643434.1:c.*1312T>C	ENSP00000494699.1:n.*1312T>C
ENST00000356231.3:c.2134T>C	ENSP00000348564.3:p.Tyr712His
ENST00000562465.5:c.127T>C	ENSP00000454246.1:p.Tyr43His
NM_138477.2:c.2134T>C	NP_612486.2:p.Tyr712His
XM_005254176.3:c.2137T>C	XP_005254233.1:p.Tyr713His
XM_011521270.1:c.2161T>C	XP_011519572.1:p.Tyr721His
XM_011521271.1:c.2158T>C	XP_011519573.1:p.Tyr720His
XM_011521272.1:c.2161T>C	XP_011519574.1:p.Tyr721His
XM_011521273.1:c.2161T>C	XP_011519575.1:p.Tyr721His
XM_011521274.1:c.1126T>C	XP_011519576.1:p.Tyr376His
XM_011521275.1:c.1378T>C	XP_011519577.1:p.Tyr460His
XR_931757.1:n.2134T>C
NM_138477.4:c.2134T>C MANE Select	NP_612486.2:p.Tyr712His
XM_005254176.5:c.2137T>C	XP_005254233.1:p.Tyr713His
XM_011521270.2:c.2161T>C	XP_011519572.1:p.Tyr721His
XM_011521271.2:c.2158T>C	XP_011519573.1:p.Tyr720His
XM_011521274.2:c.1126T>C	XP_011519576.1:p.Tyr376His
XR_001751104.1:n.2191T>C
XR_001751105.1:n.2191T>C
XR_931757.2:n.2154T>C