Canonical Allele Identifier: CA7515069

Gene: CDAN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42724509A>G , CM000677.2:g.42724509A>G	GRCh38
NC_000015.9:g.43016707A>G , CM000677.1:g.43016707A>G	GRCh37
NC_000015.8:g.40803999A>G	NCBI36
NG_012491.1:g.17711T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_138477.4:c.3666T>C MANE Select	NP_612486.2:p.Thr1222=
ENST00000356231.4:c.3666T>C MANE Select	ENSP00000348564.3:p.Thr1222=
NM_138477.2:c.3666T>C	NP_612486.2:p.Thr1222=
ENST00000356231.3:c.3666T>C	ENSP00000348564.3:p.Thr1222=
ENST00000562465.5:c.1612T>C	ENSP00000454246.1:n.1612T>C
ENST00000563604.1:n.1129T>C
ENST00000643434.1:c.*2733T>C	ENSP00000494699.1:n.*2733T>C
XM_005254176.3:c.3669T>C	XP_005254233.1:p.Thr1223=
XM_005254176.5:c.3669T>C	XP_005254233.1:p.Thr1223=
XM_011521270.1:c.3693T>C	XP_011519572.1:p.Thr1231=
XM_011521270.2:c.3693T>C	XP_011519572.1:p.Thr1231=
XM_011521271.1:c.3690T>C	XP_011519573.1:p.Thr1230=
XM_011521271.2:c.3690T>C	XP_011519573.1:p.Thr1230=
XM_011521274.1:c.2658T>C	XP_011519576.1:p.Thr886=
XM_011521274.2:c.2658T>C	XP_011519576.1:p.Thr886=
XM_011521275.1:c.2910T>C	XP_011519577.1:p.Thr970=
XR_001751104.1:n.3659T>C
XR_001751105.1:n.3676T>C