Canonical Allele Identifier: CA7515148

Gene: CDAN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42725478G>A , CM000677.2:g.42725478G>A	GRCh38
NC_000015.9:g.43017676G>A , CM000677.1:g.43017676G>A	GRCh37
NC_000015.8:g.40804968G>A	NCBI36
NG_012491.1:g.16742C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_138477.4:c.3450+11C>T MANE Select	NP_612486.2:n.3450+11C>T
ENST00000356231.4:c.3450+11C>T MANE Select	ENSP00000348564.3:n.3450+11C>T
NM_138477.2:c.3450+11C>T	NP_612486.2:n.3450+11C>T
ENST00000356231.3:c.3450+11C>T	ENSP00000348564.3:n.3450+11C>T
ENST00000562465.5:c.1396+11C>T	ENSP00000454246.1:n.1396+11C>T
ENST00000563604.1:n.160C>T
ENST00000565930.1:n.51+11C>T
ENST00000643434.1:c.*2517+11C>T	ENSP00000494699.1:n.*2517+11C>T
XM_005254176.3:c.3453+11C>T	XP_005254233.1:n.3453+11C>T
XM_005254176.5:c.3453+11C>T	XP_005254233.1:n.3453+11C>T
XM_011521270.1:c.3477+11C>T	XP_011519572.1:n.3477+11C>T
XM_011521270.2:c.3477+11C>T	XP_011519572.1:n.3477+11C>T
XM_011521271.1:c.3474+11C>T	XP_011519573.1:n.3474+11C>T
XM_011521271.2:c.3474+11C>T	XP_011519573.1:n.3474+11C>T
XM_011521274.1:c.2442+11C>T	XP_011519576.1:n.2442+11C>T
XM_011521274.2:c.2442+11C>T	XP_011519576.1:n.2442+11C>T
XM_011521275.1:c.2694+11C>T	XP_011519577.1:n.2694+11C>T
XR_001751104.1:n.3443+11C>T
XR_001751105.1:n.3460+11C>T