Canonical Allele Identifier: CA10635990

Gene: CDAN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42724142T>C , CM000677.2:g.42724142T>C	GRCh38
NC_000015.9:g.43016340T>C , CM000677.1:g.43016340T>C	GRCh37
NC_000015.8:g.40803632T>C	NCBI36
NG_012491.1:g.18078A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356231.4:c.*349A>G MANE Select	ENSP00000348564.3:n.*349A>G
ENST00000643434.1:c.*3100A>G	ENSP00000494699.1:n.*3100A>G
ENST00000356231.3:c.*349A>G	ENSP00000348564.3:n.*349A>G
ENST00000562465.5:c.1979A>G	ENSP00000454246.1:n.1979A>G
ENST00000563604.1:n.1496A>G
NM_138477.2:c.*349A>G	NP_612486.2:n.*349A>G
XM_005254176.3:c.*349A>G	XP_005254233.1:n.*349A>G
XM_011521270.1:c.*349A>G	XP_011519572.1:n.*349A>G
XM_011521271.1:c.*349A>G	XP_011519573.1:n.*349A>G
XM_011521274.1:c.*349A>G	XP_011519576.1:n.*349A>G
XM_011521275.1:c.*349A>G	XP_011519577.1:n.*349A>G
NM_138477.4:c.*349A>G MANE Select	NP_612486.2:n.*349A>G
XM_005254176.5:c.*349A>G	XP_005254233.1:n.*349A>G
XM_011521270.2:c.*349A>G	XP_011519572.1:n.*349A>G
XM_011521271.2:c.*349A>G	XP_011519573.1:n.*349A>G
XM_011521274.2:c.*349A>G	XP_011519576.1:n.*349A>G
XR_001751104.1:n.4026A>G
XR_001751105.1:n.4043A>G