Canonical Allele Identifier: CA407009075

Linked Data

dbSNP Id: rs2089510730

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50791786C>A , CM000681.2:g.50791786C>A GRCh38
NC_000019.9:g.51295043C>A , CM000681.1:g.51295043C>A GRCh37
NC_000019.8:g.55986855C>A NCBI36
NG_052652.1:g.6372C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000270593.2:c.434C>A (ACP4) MANE Select ENSP00000270593.1:p.Pro145His
ENST00000636757.1:c.-60+619G>T (SMIM47) ENSP00000489695.1:n.-60+619G>T
ENST00000270593.1:c.434C>A (ACP4) ENSP00000270593.1:p.Pro145His
NM_033068.2:c.434C>A (ACP4) NP_149059.1:p.Pro145His
XR_936026.1:n.424+619G>T
XR_936026.2:n.434+619G>T
NM_033068.3:c.434C>A (ACP4) MANE Select NP_149059.1:p.Pro145His