Canonical Allele Identifier: CA392027856

Gene: CDAN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42725593T>A , CM000677.2:g.42725593T>A	GRCh38
NC_000015.9:g.43017791T>A , CM000677.1:g.43017791T>A	GRCh37
NC_000015.8:g.40805083T>A	NCBI36
NG_012491.1:g.16627A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356231.4:c.3346A>T MANE Select	ENSP00000348564.3:p.Met1116Leu
ENST00000643434.1:c.*2413A>T	ENSP00000494699.1:n.*2413A>T
ENST00000356231.3:c.3346A>T	ENSP00000348564.3:p.Met1116Leu
ENST00000562465.5:c.1292A>T	ENSP00000454246.1:n.1292A>T
ENST00000563604.1:n.45A>T
NM_138477.2:c.3346A>T	NP_612486.2:p.Met1116Leu
XM_005254176.3:c.3349A>T	XP_005254233.1:p.Met1117Leu
XM_011521270.1:c.3373A>T	XP_011519572.1:p.Met1125Leu
XM_011521271.1:c.3370A>T	XP_011519573.1:p.Met1124Leu
XM_011521272.1:c.*54A>T	XP_011519574.1:n.*54A>T
XM_011521274.1:c.2338A>T	XP_011519576.1:p.Met780Leu
XM_011521275.1:c.2590A>T	XP_011519577.1:p.Met864Leu
NM_138477.4:c.3346A>T MANE Select	NP_612486.2:p.Met1116Leu
XM_005254176.5:c.3349A>T	XP_005254233.1:p.Met1117Leu
XM_011521270.2:c.3373A>T	XP_011519572.1:p.Met1125Leu
XM_011521271.2:c.3370A>T	XP_011519573.1:p.Met1124Leu
XM_011521274.2:c.2338A>T	XP_011519576.1:p.Met780Leu
XR_001751104.1:n.3339A>T
XR_001751105.1:n.3356A>T