Canonical Allele Identifier: CA2586620378

Gene: ACP4 SMIM47

Linked Data

• gnomAD v4: 19-50791964-G-T

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270593.2:c.451-109G>T (ACP4) MANE Select	ENSP00000270593.1:n.451-109G>T
ENST00000636757.1:c.-60+441C>A (SMIM47)	ENSP00000489695.1:n.-60+441C>A
ENST00000270593.1:c.451-109G>T (ACP4)	ENSP00000270593.1:n.451-109G>T
NM_033068.2:c.451-109G>T (ACP4)	NP_149059.1:n.451-109G>T
XR_936026.1:n.424+441C>A
XR_936026.2:n.434+441C>A
NM_033068.3:c.451-109G>T (ACP4) MANE Select	NP_149059.1:n.451-109G>T