Canonical Allele Identifier: CA2575698376

Gene: CDAN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42728981A>C , CM000677.2:g.42728981A>C	GRCh38
NC_000015.9:g.43021179A>C , CM000677.1:g.43021179A>C	GRCh37
NC_000015.8:g.40808471A>C	NCBI36
NG_012491.1:g.13239T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000356231.4:c.2645+42T>G MANE Select	ENSP00000348564.3:n.2645+42T>G
ENST00000643434.1:c.*1823+42T>G	ENSP00000494699.1:n.*1823+42T>G
ENST00000356231.3:c.2645+42T>G	ENSP00000348564.3:n.2645+42T>G
ENST00000562465.5:c.638+42T>G	ENSP00000454246.1:n.638+42T>G
NM_138477.2:c.2645+42T>G	NP_612486.2:n.2645+42T>G
XM_005254176.3:c.2648+42T>G	XP_005254233.1:n.2648+42T>G
XM_011521270.1:c.2672+42T>G	XP_011519572.1:n.2672+42T>G
XM_011521271.1:c.2669+42T>G	XP_011519573.1:n.2669+42T>G
XM_011521272.1:c.2672+42T>G	XP_011519574.1:n.2672+42T>G
XM_011521273.1:c.2672+42T>G	XP_011519575.1:n.2672+42T>G
XM_011521274.1:c.1637+42T>G	XP_011519576.1:n.1637+42T>G
XM_011521275.1:c.1889+42T>G	XP_011519577.1:n.1889+42T>G
NM_138477.4:c.2645+42T>G MANE Select	NP_612486.2:n.2645+42T>G
XM_005254176.5:c.2648+42T>G	XP_005254233.1:n.2648+42T>G
XM_011521270.2:c.2672+42T>G	XP_011519572.1:n.2672+42T>G
XM_011521271.2:c.2669+42T>G	XP_011519573.1:n.2669+42T>G
XM_011521274.2:c.1637+42T>G	XP_011519576.1:n.1637+42T>G
XR_001751104.1:n.2702+42T>G
XR_001751105.1:n.2702+42T>G