Canonical Allele Identifier: CA2735999367

Gene: ACP4 SMIM47

Linked Data

• dbSNP Id: rs2123288565

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50791923A>C , CM000681.2:g.50791923A>C	GRCh38
NC_000019.9:g.51295180A>C , CM000681.1:g.51295180A>C	GRCh37
NC_000019.8:g.55986992A>C	NCBI36
NG_052652.1:g.6509A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270593.2:c.450+121A>C (ACP4) MANE Select	ENSP00000270593.1:n.450+121A>C
ENST00000636757.1:c.-60+482T>G (SMIM47)	ENSP00000489695.1:n.-60+482T>G
ENST00000270593.1:c.450+121A>C (ACP4)	ENSP00000270593.1:n.450+121A>C
NM_033068.2:c.450+121A>C (ACP4)	NP_149059.1:n.450+121A>C
XR_936026.1:n.424+482T>G
XR_936026.2:n.434+482T>G
NM_033068.3:c.450+121A>C (ACP4) MANE Select	NP_149059.1:n.450+121A>C