Canonical Allele Identifier: CA407009152
Gene: ACP4 HGNC NCBI
SMIM47 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.51295058A>G (hg19) chr19:g.50791801A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50791801A>G , CM000681.2:g.50791801A>G GRCh38
NC_000019.9:g.51295058A>G , CM000681.1:g.51295058A>G GRCh37
NC_000019.8:g.55986870A>G NCBI36
NG_052652.1:g.6387A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000270593.2:c.449A>G (ACP4) MANE Select ENSP00000270593.1:p.Lys150Arg
ENST00000636757.1:c.-60+604T>C (SMIM47) ENSP00000489695.1:n.-60+604T>C
ENST00000270593.1:c.449A>G (ACP4) ENSP00000270593.1:p.Lys150Arg
NM_033068.2:c.449A>G (ACP4) NP_149059.1:p.Lys150Arg
XR_936026.1:n.424+604T>C
XR_936026.2:n.434+604T>C
NM_033068.3:c.449A>G (ACP4) MANE Select NP_149059.1:p.Lys150Arg
Search 100 bp 5'
Search 100 bp 3'