Canonical Allele Identifier: CA2341080364
Gene: ACP4 HGNC NCBI
SMIM47 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50791582T= , CM000681.2:g.50791582T= GRCh38
NC_000019.9:g.51294839T= , CM000681.1:g.51294839T= GRCh37
NC_000019.8:g.55986651T= NCBI36
NG_052652.1:g.6168T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000270593.2:c.304-74T= (ACP4) MANE Select ENSP00000270593.1:n.304-74T=
ENST00000636757.1:c.-60+823A= (SMIM47) ENSP00000489695.1:n.-60+823A=
ENST00000270593.1:c.304-74T= (ACP4) ENSP00000270593.1:n.304-74T=
NM_033068.2:c.304-74T= (ACP4) NP_149059.1:n.304-74T=
XR_936026.1:n.424+823A=
XR_936026.2:n.434+823A=
NM_033068.3:c.304-74T= (ACP4) MANE Select NP_149059.1:n.304-74T=
Search 100 bp 5'
Search 100 bp 3'