Canonical Allele Identifier: CA2735999358

Gene: ACP4 SMIM47

Linked Data

• dbSNP Id: rs2123288503

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50791893G>A , CM000681.2:g.50791893G>A	GRCh38
NC_000019.9:g.51295150G>A , CM000681.1:g.51295150G>A	GRCh37
NC_000019.8:g.55986962G>A	NCBI36
NG_052652.1:g.6479G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270593.2:c.450+91G>A (ACP4) MANE Select	ENSP00000270593.1:n.450+91G>A
ENST00000636757.1:c.-60+512C>T (SMIM47)	ENSP00000489695.1:n.-60+512C>T
ENST00000270593.1:c.450+91G>A (ACP4)	ENSP00000270593.1:n.450+91G>A
NM_033068.2:c.450+91G>A (ACP4)	NP_149059.1:n.450+91G>A
XR_936026.1:n.424+512C>T
XR_936026.2:n.434+512C>T
NM_033068.3:c.450+91G>A (ACP4) MANE Select	NP_149059.1:n.450+91G>A