Canonical Allele Identifier: CA2586620234

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50791803del , CM000681.2:g.50791803del GRCh38
NC_000019.9:g.51295060del , CM000681.1:g.51295060del GRCh37
NC_000019.8:g.55986872del NCBI36
NG_052652.1:g.6389del

Transcript Alleles

HGVS Amino-acid Change
ENST00000270593.2:c.450+1del (ACP4)
ENST00000636757.1:c.-60+603del (SMIM47) ENSP00000489695.1:n.-60+603del
ENST00000270593.1:c.450+1del (ACP4)
NM_033068.2:c.450+1del (ACP4)
XR_936026.1:n.424+603del
XR_936026.2:n.434+603del
NM_033068.3:c.450+1del (ACP4)