Canonical Allele Identifier: CA490002034

Gene: CDAN1

Linked Data

• gnomAD v4: 15-42731217-G-A
• MyVariant Identifiers: chr15:g.43023415G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42731217G>A , CM000677.2:g.42731217G>A	GRCh38
NC_000015.9:g.43023415G>A , CM000677.1:g.43023415G>A	GRCh37
NC_000015.8:g.40810707G>A	NCBI36
NG_012491.1:g.11003C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000356231.4:c.1854C>T MANE Select	ENSP00000348564.3:p.Asp618=
ENST00000643434.1:c.*1032C>T	ENSP00000494699.1:n.*1032C>T
ENST00000356231.3:c.1854C>T	ENSP00000348564.3:p.Asp618=
NM_138477.2:c.1854C>T	NP_612486.2:p.Asp618=
XM_005254176.3:c.1857C>T	XP_005254233.1:p.Asp619=
XM_011521270.1:c.1881C>T	XP_011519572.1:p.Asp627=
XM_011521271.1:c.1878C>T	XP_011519573.1:p.Asp626=
XM_011521272.1:c.1881C>T	XP_011519574.1:p.Asp627=
XM_011521273.1:c.1881C>T	XP_011519575.1:p.Asp627=
XM_011521274.1:c.846C>T	XP_011519576.1:p.Asp282=
XM_011521275.1:c.1098C>T	XP_011519577.1:p.Asp366=
XR_931757.1:n.1892C>T
NM_138477.4:c.1854C>T MANE Select	NP_612486.2:p.Asp618=
XM_005254176.5:c.1857C>T	XP_005254233.1:p.Asp619=
XM_011521270.2:c.1881C>T	XP_011519572.1:p.Asp627=
XM_011521271.2:c.1878C>T	XP_011519573.1:p.Asp626=
XM_011521274.2:c.846C>T	XP_011519576.1:p.Asp282=
XR_001751104.1:n.1911C>T
XR_001751105.1:n.1911C>T
XR_931757.2:n.1912C>T