Canonical Allele Identifier: CA2564044064

Gene: ACP4 SMIM47

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50791952T>C , CM000681.2:g.50791952T>C	GRCh38
NC_000019.9:g.51295209T>C , CM000681.1:g.51295209T>C	GRCh37
NC_000019.8:g.55987021T>C	NCBI36
NG_052652.1:g.6538T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270593.2:c.451-121T>C (ACP4) MANE Select	ENSP00000270593.1:n.451-121T>C
ENST00000636757.1:c.-60+453A>G (SMIM47)	ENSP00000489695.1:n.-60+453A>G
ENST00000270593.1:c.451-121T>C (ACP4)	ENSP00000270593.1:n.451-121T>C
NM_033068.2:c.451-121T>C (ACP4)	NP_149059.1:n.451-121T>C
XR_936026.1:n.424+453A>G
XR_936026.2:n.434+453A>G
NM_033068.3:c.451-121T>C (ACP4) MANE Select	NP_149059.1:n.451-121T>C