Canonical Allele Identifier: CA7515923

Gene: CDAN1

Linked Data

• ClinVar Variation Id: 885242
• ClinVar RCV Id: RCV001116709 ; RCV002556471 ; RCV003145349
• dbSNP Id: rs146810840
• ExAC: 15:43023447 G / A
• gnomAD v2: 15-43023447-G-A
• gnomAD v3: 15-42731249-G-A
• gnomAD v4: 15-42731249-G-A
• MyVariant Identifiers: chr15:g.43023447G>A (hg19) ; chr15:g.42731249G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42731249G>A , CM000677.2:g.42731249G>A	GRCh38
NC_000015.9:g.43023447G>A , CM000677.1:g.43023447G>A	GRCh37
NC_000015.8:g.40810739G>A	NCBI36
NG_012491.1:g.10971C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356231.4:c.1822C>T MANE Select	ENSP00000348564.3:p.Pro608Ser
ENST00000643434.1:c.*1000C>T	ENSP00000494699.1:n.*1000C>T
ENST00000356231.3:c.1822C>T	ENSP00000348564.3:p.Pro608Ser
NM_138477.2:c.1822C>T	NP_612486.2:p.Pro608Ser
XM_005254176.3:c.1825C>T	XP_005254233.1:p.Pro609Ser
XM_011521270.1:c.1849C>T	XP_011519572.1:p.Pro617Ser
XM_011521271.1:c.1846C>T	XP_011519573.1:p.Pro616Ser
XM_011521272.1:c.1849C>T	XP_011519574.1:p.Pro617Ser
XM_011521273.1:c.1849C>T	XP_011519575.1:p.Pro617Ser
XM_011521274.1:c.814C>T	XP_011519576.1:p.Pro272Ser
XM_011521275.1:c.1066C>T	XP_011519577.1:p.Pro356Ser
XR_931757.1:n.1860C>T
NM_138477.4:c.1822C>T MANE Select	NP_612486.2:p.Pro608Ser
XM_005254176.5:c.1825C>T	XP_005254233.1:p.Pro609Ser
XM_011521270.2:c.1849C>T	XP_011519572.1:p.Pro617Ser
XM_011521271.2:c.1846C>T	XP_011519573.1:p.Pro616Ser
XM_011521274.2:c.814C>T	XP_011519576.1:p.Pro272Ser
XR_001751104.1:n.1879C>T
XR_001751105.1:n.1879C>T
XR_931757.2:n.1880C>T