Canonical Allele Identifier: CA392044736

Gene: CDAN1

Linked Data

• ClinVar Variation Id: 1714380
• ClinVar RCV Id: RCV002297318
• gnomAD v4: 15-42731255-G-A
• MyVariant Identifiers: chr15:g.43023453G>A (hg19) ; chr15:g.42731255G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42731255G>A , CM000677.2:g.42731255G>A	GRCh38
NC_000015.9:g.43023453G>A , CM000677.1:g.43023453G>A	GRCh37
NC_000015.8:g.40810745G>A	NCBI36
NG_012491.1:g.10965C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356231.4:c.1816C>T MANE Select	ENSP00000348564.3:p.His606Tyr
ENST00000643434.1:c.*994C>T	ENSP00000494699.1:n.*994C>T
ENST00000356231.3:c.1816C>T	ENSP00000348564.3:p.His606Tyr
NM_138477.2:c.1816C>T	NP_612486.2:p.His606Tyr
XM_005254176.3:c.1819C>T	XP_005254233.1:p.His607Tyr
XM_011521270.1:c.1843C>T	XP_011519572.1:p.His615Tyr
XM_011521271.1:c.1840C>T	XP_011519573.1:p.His614Tyr
XM_011521272.1:c.1843C>T	XP_011519574.1:p.His615Tyr
XM_011521273.1:c.1843C>T	XP_011519575.1:p.His615Tyr
XM_011521274.1:c.808C>T	XP_011519576.1:p.His270Tyr
XM_011521275.1:c.1060C>T	XP_011519577.1:p.His354Tyr
XR_931757.1:n.1854C>T
NM_138477.4:c.1816C>T MANE Select	NP_612486.2:p.His606Tyr
XM_005254176.5:c.1819C>T	XP_005254233.1:p.His607Tyr
XM_011521270.2:c.1843C>T	XP_011519572.1:p.His615Tyr
XM_011521271.2:c.1840C>T	XP_011519573.1:p.His614Tyr
XM_011521274.2:c.808C>T	XP_011519576.1:p.His270Tyr
XR_001751104.1:n.1873C>T
XR_001751105.1:n.1873C>T
XR_931757.2:n.1874C>T