Canonical Allele Identifier: CA392037080

Gene: CDAN1

Linked Data

• gnomAD v4: 15-42729074-G-A
• MyVariant Identifiers: chr15:g.43021272G>A (hg19) ; chr15:g.42729074G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42729074G>A , CM000677.2:g.42729074G>A	GRCh38
NC_000015.9:g.43021272G>A , CM000677.1:g.43021272G>A	GRCh37
NC_000015.8:g.40808564G>A	NCBI36
NG_012491.1:g.13146C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000356231.4:c.2594C>T MANE Select	ENSP00000348564.3:p.Thr865Ile
ENST00000643434.1:c.*1772C>T	ENSP00000494699.1:n.*1772C>T
ENST00000356231.3:c.2594C>T	ENSP00000348564.3:p.Thr865Ile
ENST00000562465.5:c.587C>T	ENSP00000454246.1:p.Thr196Ile
NM_138477.2:c.2594C>T	NP_612486.2:p.Thr865Ile
XM_005254176.3:c.2597C>T	XP_005254233.1:p.Thr866Ile
XM_011521270.1:c.2621C>T	XP_011519572.1:p.Thr874Ile
XM_011521271.1:c.2618C>T	XP_011519573.1:p.Thr873Ile
XM_011521272.1:c.2621C>T	XP_011519574.1:p.Thr874Ile
XM_011521273.1:c.2621C>T	XP_011519575.1:p.Thr874Ile
XM_011521274.1:c.1586C>T	XP_011519576.1:p.Thr529Ile
XM_011521275.1:c.1838C>T	XP_011519577.1:p.Thr613Ile
NM_138477.4:c.2594C>T MANE Select	NP_612486.2:p.Thr865Ile
XM_005254176.5:c.2597C>T	XP_005254233.1:p.Thr866Ile
XM_011521270.2:c.2621C>T	XP_011519572.1:p.Thr874Ile
XM_011521271.2:c.2618C>T	XP_011519573.1:p.Thr873Ile
XM_011521274.2:c.1586C>T	XP_011519576.1:p.Thr529Ile
XR_001751104.1:n.2651C>T
XR_001751105.1:n.2651C>T