Canonical Allele Identifier: CA618002264

Gene: CDAN1

Linked Data

• dbSNP Id: rs1289448267
• gnomAD v2: 15-43023309-G-A
• gnomAD v4: 15-42731111-G-A
• MyVariant Identifiers: chr15:g.43023309G>A (hg19) ; chr15:g.42731111G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42731111G>A , CM000677.2:g.42731111G>A	GRCh38
NC_000015.9:g.43023309G>A , CM000677.1:g.43023309G>A	GRCh37
NC_000015.8:g.40810601G>A	NCBI36
NG_012491.1:g.11109C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356231.4:c.1861-40C>T MANE Select	ENSP00000348564.3:n.1861-40C>T
ENST00000643434.1:c.*1039-40C>T	ENSP00000494699.1:n.*1039-40C>T
ENST00000356231.3:c.1861-40C>T	ENSP00000348564.3:n.1861-40C>T
NM_138477.2:c.1861-40C>T	NP_612486.2:n.1861-40C>T
XM_005254176.3:c.1864-40C>T	XP_005254233.1:n.1864-40C>T
XM_011521270.1:c.1888-40C>T	XP_011519572.1:n.1888-40C>T
XM_011521271.1:c.1885-40C>T	XP_011519573.1:n.1885-40C>T
XM_011521272.1:c.1888-40C>T	XP_011519574.1:n.1888-40C>T
XM_011521273.1:c.1888-40C>T	XP_011519575.1:n.1888-40C>T
XM_011521274.1:c.853-40C>T	XP_011519576.1:n.853-40C>T
XM_011521275.1:c.1105-40C>T	XP_011519577.1:n.1105-40C>T
XR_931757.1:n.1899-40C>T
NM_138477.4:c.1861-40C>T MANE Select	NP_612486.2:n.1861-40C>T
XM_005254176.5:c.1864-40C>T	XP_005254233.1:n.1864-40C>T
XM_011521270.2:c.1888-40C>T	XP_011519572.1:n.1888-40C>T
XM_011521271.2:c.1885-40C>T	XP_011519573.1:n.1885-40C>T
XM_011521274.2:c.853-40C>T	XP_011519576.1:n.853-40C>T
XR_001751104.1:n.1918-40C>T
XR_001751105.1:n.1918-40C>T
XR_931757.2:n.1919-40C>T