Canonical Allele Identifier: CA489895198

Gene: CDAN1

Linked Data

• ClinVar Variation Id: 2863722
• ClinVar RCV Id: RCV003702419
• dbSNP Id: rs2061598382
• gnomAD v4: 15-42730636-A-G
• MyVariant Identifiers: chr15:g.43022834A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42730636A>G , CM000677.2:g.42730636A>G	GRCh38
NC_000015.9:g.43022834A>G , CM000677.1:g.43022834A>G	GRCh37
NC_000015.8:g.40810126A>G	NCBI36
NG_012491.1:g.11584T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000356231.4:c.2136T>C MANE Select	ENSP00000348564.3:p.Tyr712=
ENST00000643434.1:c.*1314T>C	ENSP00000494699.1:n.*1314T>C
ENST00000356231.3:c.2136T>C	ENSP00000348564.3:p.Tyr712=
ENST00000562465.5:c.129T>C	ENSP00000454246.1:p.Tyr43=
NM_138477.2:c.2136T>C	NP_612486.2:p.Tyr712=
XM_005254176.3:c.2139T>C	XP_005254233.1:p.Tyr713=
XM_011521270.1:c.2163T>C	XP_011519572.1:p.Tyr721=
XM_011521271.1:c.2160T>C	XP_011519573.1:p.Tyr720=
XM_011521272.1:c.2163T>C	XP_011519574.1:p.Tyr721=
XM_011521273.1:c.2163T>C	XP_011519575.1:p.Tyr721=
XM_011521274.1:c.1128T>C	XP_011519576.1:p.Tyr376=
XM_011521275.1:c.1380T>C	XP_011519577.1:p.Tyr460=
XR_931757.1:n.2136T>C
NM_138477.4:c.2136T>C MANE Select	NP_612486.2:p.Tyr712=
XM_005254176.5:c.2139T>C	XP_005254233.1:p.Tyr713=
XM_011521270.2:c.2163T>C	XP_011519572.1:p.Tyr721=
XM_011521271.2:c.2160T>C	XP_011519573.1:p.Tyr720=
XM_011521274.2:c.1128T>C	XP_011519576.1:p.Tyr376=
XR_001751104.1:n.2193T>C
XR_001751105.1:n.2193T>C
XR_931757.2:n.2156T>C