Canonical Allele Identifier: CA2341080514
Gene: ACP4 HGNC NCBI
SMIM47 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50791834A= , CM000681.2:g.50791834A= GRCh38
NC_000019.9:g.51295091A= , CM000681.1:g.51295091A= GRCh37
NC_000019.8:g.55986903A= NCBI36
NG_052652.1:g.6420A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000270593.2:c.450+32A= (ACP4) MANE Select ENSP00000270593.1:n.450+32A=
ENST00000636757.1:c.-60+571T= (SMIM47) ENSP00000489695.1:n.-60+571T=
ENST00000270593.1:c.450+32A= (ACP4) ENSP00000270593.1:n.450+32A=
NM_033068.2:c.450+32A= (ACP4) NP_149059.1:n.450+32A=
XR_936026.1:n.424+571T=
XR_936026.2:n.434+571T=
NM_033068.3:c.450+32A= (ACP4) MANE Select NP_149059.1:n.450+32A=
Search 100 bp 5'
Search 100 bp 3'