Canonical Allele Identifier: CA392024477

Gene: CDAN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42724492T>C , CM000677.2:g.42724492T>C	GRCh38
NC_000015.9:g.43016690T>C , CM000677.1:g.43016690T>C	GRCh37
NC_000015.8:g.40803982T>C	NCBI36
NG_012491.1:g.17728A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356231.4:c.3683A>G MANE Select	ENSP00000348564.3:p.Ter1228Trp
ENST00000643434.1:c.*2750A>G	ENSP00000494699.1:n.*2750A>G
ENST00000356231.3:c.3683A>G	ENSP00000348564.3:p.Ter1228Trp
ENST00000562465.5:c.1629A>G	ENSP00000454246.1:n.1629A>G
ENST00000563604.1:n.1146A>G
NM_138477.2:c.3683A>G	NP_612486.2:p.Ter1228Trp
XM_005254176.3:c.3686A>G	XP_005254233.1:p.Ter1229Trp
XM_011521270.1:c.3710A>G	XP_011519572.1:p.Ter1237Trp
XM_011521271.1:c.3707A>G	XP_011519573.1:p.Ter1236Trp
XM_011521274.1:c.2675A>G	XP_011519576.1:p.Ter892Trp
XM_011521275.1:c.2927A>G	XP_011519577.1:p.Ter976Trp
NM_138477.4:c.3683A>G MANE Select	NP_612486.2:p.Ter1228Trp
XM_005254176.5:c.3686A>G	XP_005254233.1:p.Ter1229Trp
XM_011521270.2:c.3710A>G	XP_011519572.1:p.Ter1237Trp
XM_011521271.2:c.3707A>G	XP_011519573.1:p.Ter1236Trp
XM_011521274.2:c.2675A>G	XP_011519576.1:p.Ter892Trp
XR_001751104.1:n.3676A>G
XR_001751105.1:n.3693A>G