Canonical Allele Identifier: CA7515249

Gene: CDAN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42726305C>T , CM000677.2:g.42726305C>T	GRCh38
NC_000015.9:g.43018503C>T , CM000677.1:g.43018503C>T	GRCh37
NC_000015.8:g.40805795C>T	NCBI36
NG_012491.1:g.15915G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_138477.4:c.3204+5G>A MANE Select	NP_612486.2:n.3204+5G>A
ENST00000356231.4:c.3204+5G>A MANE Select	ENSP00000348564.3:n.3204+5G>A
NM_138477.2:c.3204+5G>A	NP_612486.2:n.3204+5G>A
ENST00000356231.3:c.3204+5G>A	ENSP00000348564.3:n.3204+5G>A
ENST00000562465.5:c.1150+5G>A	ENSP00000454246.1:n.1150+5G>A
ENST00000643434.1:c.*2335+5G>A	ENSP00000494699.1:n.*2335+5G>A
XM_005254176.3:c.3207+5G>A	XP_005254233.1:n.3207+5G>A
XM_005254176.5:c.3207+5G>A	XP_005254233.1:n.3207+5G>A
XM_011521270.1:c.3231+5G>A	XP_011519572.1:n.3231+5G>A
XM_011521270.2:c.3231+5G>A	XP_011519572.1:n.3231+5G>A
XM_011521271.1:c.3228+5G>A	XP_011519573.1:n.3228+5G>A
XM_011521271.2:c.3228+5G>A	XP_011519573.1:n.3228+5G>A
XM_011521272.1:c.3231+5G>A	XP_011519574.1:n.3231+5G>A
XM_011521274.1:c.2196+5G>A	XP_011519576.1:n.2196+5G>A
XM_011521274.2:c.2196+5G>A	XP_011519576.1:n.2196+5G>A
XM_011521275.1:c.2448+5G>A	XP_011519577.1:n.2448+5G>A
XR_001751104.1:n.3261+5G>A
XR_001751105.1:n.3214+5G>A