Canonical Allele Identifier: CA7515847

Gene: CDAN1

Linked Data

• ClinVar Variation Id: 315940
• ClinVar RCV Id: RCV000342376 ; RCV000925695
• dbSNP Id: rs201733620
• ExAC: 15:43022970 G / A
• gnomAD v2: 15-43022970-G-A
• gnomAD v3: 15-42730772-G-A
• gnomAD v4: 15-42730772-G-A
• MyVariant Identifiers: chr15:g.43022970G>A (hg19) ; chr15:g.42730772G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42730772G>A , CM000677.2:g.42730772G>A	GRCh38
NC_000015.9:g.43022970G>A , CM000677.1:g.43022970G>A	GRCh37
NC_000015.8:g.40810262G>A	NCBI36
NG_012491.1:g.11448C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356231.4:c.2008-8C>T MANE Select	ENSP00000348564.3:n.2008-8C>T
ENST00000643434.1:c.*1186-8C>T	ENSP00000494699.1:n.*1186-8C>T
ENST00000356231.3:c.2008-8C>T	ENSP00000348564.3:n.2008-8C>T
NM_138477.2:c.2008-8C>T	NP_612486.2:n.2008-8C>T
XM_005254176.3:c.2011-8C>T	XP_005254233.1:n.2011-8C>T
XM_011521270.1:c.2035-8C>T	XP_011519572.1:n.2035-8C>T
XM_011521271.1:c.2032-8C>T	XP_011519573.1:n.2032-8C>T
XM_011521272.1:c.2035-8C>T	XP_011519574.1:n.2035-8C>T
XM_011521273.1:c.2035-8C>T	XP_011519575.1:n.2035-8C>T
XM_011521274.1:c.1000-8C>T	XP_011519576.1:n.1000-8C>T
XM_011521275.1:c.1252-8C>T	XP_011519577.1:n.1252-8C>T
XR_931757.1:n.2008-8C>T
NM_138477.4:c.2008-8C>T MANE Select	NP_612486.2:n.2008-8C>T
XM_005254176.5:c.2011-8C>T	XP_005254233.1:n.2011-8C>T
XM_011521270.2:c.2035-8C>T	XP_011519572.1:n.2035-8C>T
XM_011521271.2:c.2032-8C>T	XP_011519573.1:n.2032-8C>T
XM_011521274.2:c.1000-8C>T	XP_011519576.1:n.1000-8C>T
XR_001751104.1:n.2065-8C>T
XR_001751105.1:n.2065-8C>T
XR_931757.2:n.2028-8C>T