Canonical Allele Identifier: CA392044986

Gene: CDAN1

Linked Data

• MyVariant Identifiers: chr15:g.43023487C>G (hg19) ; chr15:g.42731289C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42731289C>G , CM000677.2:g.42731289C>G	GRCh38
NC_000015.9:g.43023487C>G , CM000677.1:g.43023487C>G	GRCh37
NC_000015.8:g.40810779C>G	NCBI36
NG_012491.1:g.10931G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356231.4:c.1782G>C MANE Select	ENSP00000348564.3:p.Lys594Asn
ENST00000643434.1:c.*960G>C	ENSP00000494699.1:n.*960G>C
ENST00000356231.3:c.1782G>C	ENSP00000348564.3:p.Lys594Asn
NM_138477.2:c.1782G>C	NP_612486.2:p.Lys594Asn
XM_005254176.3:c.1785G>C	XP_005254233.1:p.Lys595Asn
XM_011521270.1:c.1809G>C	XP_011519572.1:p.Lys603Asn
XM_011521271.1:c.1806G>C	XP_011519573.1:p.Lys602Asn
XM_011521272.1:c.1809G>C	XP_011519574.1:p.Lys603Asn
XM_011521273.1:c.1809G>C	XP_011519575.1:p.Lys603Asn
XM_011521274.1:c.774G>C	XP_011519576.1:p.Lys258Asn
XM_011521275.1:c.1026G>C	XP_011519577.1:p.Lys342Asn
XR_931757.1:n.1820G>C
NM_138477.4:c.1782G>C MANE Select	NP_612486.2:p.Lys594Asn
XM_005254176.5:c.1785G>C	XP_005254233.1:p.Lys595Asn
XM_011521270.2:c.1809G>C	XP_011519572.1:p.Lys603Asn
XM_011521271.2:c.1806G>C	XP_011519573.1:p.Lys602Asn
XM_011521274.2:c.774G>C	XP_011519576.1:p.Lys258Asn
XR_001751104.1:n.1839G>C
XR_001751105.1:n.1839G>C
XR_931757.2:n.1840G>C