Canonical Allele Identifier: CA7515268
Community Standard Title: NM_138477.4(CDAN1):c.3135C>T (p.Asp1045=)
Gene: CDAN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42726379G>A , CM000677.2:g.42726379G>A GRCh38
NC_000015.9:g.43018577G>A , CM000677.1:g.43018577G>A GRCh37
NC_000015.8:g.40805869G>A NCBI36
NG_012491.1:g.15841C>T

Transcript Alleles

HGVS Amino-acid Change
NM_138477.4:c.3135C>T MANE Select NP_612486.2:p.Asp1045=
ENST00000356231.4:c.3135C>T MANE Select ENSP00000348564.3:p.Asp1045=
NM_138477.2:c.3135C>T NP_612486.2:p.Asp1045=
ENST00000356231.3:c.3135C>T ENSP00000348564.3:p.Asp1045=
ENST00000562465.5:c.1081C>T ENSP00000454246.1:n.1081C>T
ENST00000643434.1:c.*2266C>T ENSP00000494699.1:n.*2266C>T
XM_005254176.3:c.3138C>T XP_005254233.1:p.Asp1046=
XM_005254176.5:c.3138C>T XP_005254233.1:p.Asp1046=
XM_011521270.1:c.3162C>T XP_011519572.1:p.Asp1054=
XM_011521270.2:c.3162C>T XP_011519572.1:p.Asp1054=
XM_011521271.1:c.3159C>T XP_011519573.1:p.Asp1053=
XM_011521271.2:c.3159C>T XP_011519573.1:p.Asp1053=
XM_011521272.1:c.3162C>T XP_011519574.1:p.Asp1054=
XM_011521273.1:c.*37C>T XP_011519575.1:n.*37C>T
XM_011521274.1:c.2127C>T XP_011519576.1:p.Asp709=
XM_011521274.2:c.2127C>T XP_011519576.1:p.Asp709=
XM_011521275.1:c.2379C>T XP_011519577.1:p.Asp793=
XR_001751104.1:n.3192C>T
XR_001751105.1:n.3145C>T