Canonical Allele Identifier: CA2341080414

Gene: ACP4 SMIM47

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50791679T= , CM000681.2:g.50791679T=	GRCh38
NC_000019.9:g.51294936T= , CM000681.1:g.51294936T=	GRCh37
NC_000019.8:g.55986748T=	NCBI36
NG_052652.1:g.6265T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270593.2:c.327T= (ACP4) MANE Select	ENSP00000270593.1:p.Phe109=
ENST00000636757.1:c.-60+726A= (SMIM47)	ENSP00000489695.1:n.-60+726A=
ENST00000270593.1:c.327T= (ACP4)	ENSP00000270593.1:p.Phe109=
NM_033068.2:c.327T= (ACP4)	NP_149059.1:p.Phe109=
XR_936026.1:n.424+726A=
XR_936026.2:n.434+726A=
NM_033068.3:c.327T= (ACP4) MANE Select	NP_149059.1:p.Phe109=