Canonical Allele Identifier: CA2586620373

Gene: ACP4 SMIM47

Linked Data

• gnomAD v4: 19-50791961-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50791964del , CM000681.2:g.50791964del	GRCh38
NC_000019.9:g.51295221del , CM000681.1:g.51295221del	GRCh37
NC_000019.8:g.55987033del	NCBI36
NG_052652.1:g.6550del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270593.2:c.451-109del (ACP4) MANE Select	ENSP00000270593.1:n.451-109del
ENST00000636757.1:c.-60+443del (SMIM47)	ENSP00000489695.1:n.-60+443del
ENST00000270593.1:c.451-109del (ACP4)	ENSP00000270593.1:n.451-109del
NM_033068.2:c.451-109del (ACP4)	NP_149059.1:n.451-109del
XR_936026.1:n.424+443del
XR_936026.2:n.434+443del
NM_033068.3:c.451-109del (ACP4) MANE Select	NP_149059.1:n.451-109del