Canonical Allele Identifier: CA7515380

Gene: CDAN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42727965G>A , CM000677.2:g.42727965G>A	GRCh38
NC_000015.9:g.43020163G>A , CM000677.1:g.43020163G>A	GRCh37
NC_000015.8:g.40807455G>A	NCBI36
NG_012491.1:g.14255C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_138477.4:c.2937C>T MANE Select	NP_612486.2:p.Ala979=
ENST00000356231.4:c.2937C>T MANE Select	ENSP00000348564.3:p.Ala979=
NM_138477.2:c.2937C>T	NP_612486.2:p.Ala979=
ENST00000356231.3:c.2937C>T	ENSP00000348564.3:p.Ala979=
ENST00000562465.5:c.930C>T	ENSP00000454246.1:p.Ala310=
ENST00000643434.1:c.*2115C>T	ENSP00000494699.1:n.*2115C>T
XM_005254176.3:c.2940C>T	XP_005254233.1:p.Ala980=
XM_005254176.5:c.2940C>T	XP_005254233.1:p.Ala980=
XM_011521270.1:c.2964C>T	XP_011519572.1:p.Ala988=
XM_011521270.2:c.2964C>T	XP_011519572.1:p.Ala988=
XM_011521271.1:c.2961C>T	XP_011519573.1:p.Ala987=
XM_011521271.2:c.2961C>T	XP_011519573.1:p.Ala987=
XM_011521272.1:c.2964C>T	XP_011519574.1:p.Ala988=
XM_011521273.1:c.2964C>T	XP_011519575.1:p.Ala988=
XM_011521274.1:c.1929C>T	XP_011519576.1:p.Ala643=
XM_011521274.2:c.1929C>T	XP_011519576.1:p.Ala643=
XM_011521275.1:c.2181C>T	XP_011519577.1:p.Ala727=
XR_001751104.1:n.2994C>T
XR_001751105.1:n.2994C>T