Canonical Allele Identifier: CA358348588

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.145111062T>A , CM000666.2:g.145111062T>A GRCh38
NC_000004.11:g.146032214T>A , CM000666.1:g.146032214T>A GRCh37
NC_000004.10:g.146251664T>A NCBI36
NG_047075.1:g.18059T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000296577.9:c.708T>A (ABCE1) MANE Select ENSP00000296577.4:p.Asp236Glu
ENST00000296577.8:c.708T>A (ABCE1) ENSP00000296577.4:p.Asp236Glu
ENST00000455611.6:n.2274A>T (OTUD4)
ENST00000502803.5:n.239+6547T>A (ABCE1)
ENST00000504292.1:c.412+618T>A (ABCE1) ENSP00000423415.1:n.412+618T>A
ENST00000506506.5:n.107-11959T>A (ABCE1)
ENST00000507193.5:c.708T>A (ABCE1) ENSP00000422068.1:p.Asp236Glu
NM_001040876.1:c.708T>A (ABCE1) NP_001035809.1:p.Asp236Glu
NM_002940.2:c.708T>A (ABCE1) NP_002931.2:p.Asp236Glu
NM_002940.3:c.708T>A (ABCE1) MANE Select NP_002931.2:p.Asp236Glu
NM_001040876.2:c.708T>A (ABCE1) NP_001035809.1:p.Asp236Glu