Canonical Allele Identifier: CA883239661

Gene: ACP4 SMIM47

Linked Data

• dbSNP Id: rs1173526484
• gnomAD v3: 19-50791962-G-C
• gnomAD v4: 19-50791962-G-C
• MyVariant Identifiers: chr19:g.51295219G>C (hg19) ; chr19:g.50791962G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50791962G>C , CM000681.2:g.50791962G>C	GRCh38
NC_000019.9:g.51295219G>C , CM000681.1:g.51295219G>C	GRCh37
NC_000019.8:g.55987031G>C	NCBI36
NG_052652.1:g.6548G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270593.2:c.451-111G>C (ACP4) MANE Select	ENSP00000270593.1:n.451-111G>C
ENST00000636757.1:c.-60+443C>G (SMIM47)	ENSP00000489695.1:n.-60+443C>G
ENST00000270593.1:c.451-111G>C (ACP4)	ENSP00000270593.1:n.451-111G>C
NM_033068.2:c.451-111G>C (ACP4)	NP_149059.1:n.451-111G>C
XR_936026.1:n.424+443C>G
XR_936026.2:n.434+443C>G
NM_033068.3:c.451-111G>C (ACP4) MANE Select	NP_149059.1:n.451-111G>C