Canonical Allele Identifier: CA358374562
Gene: PABPC4L HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134200368T>G , CM000666.2:g.134200368T>G GRCh38
NC_000004.11:g.135121523T>G , CM000666.1:g.135121523T>G GRCh37
NC_000004.10:g.135340973T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000421491.4:c.652A>C MANE Select ENSP00000463233.1:p.Ser218Arg
ENST00000421491.3:c.652A>C ENSP00000463233.1:p.Ser218Arg
NM_001114734.1:c.826A>C NP_001108206.2:p.Ser276Arg
NM_001114734.2:c.652A>C MANE Select NP_001108206.3:p.Ser218Arg
NM_001363585.1:c.652A>C NP_001350514.1:p.Ser218Arg
XR_001741133.1:n.1191A>C
XR_001741134.1:n.1191A>C
XR_001741135.1:n.1191A>C
XR_001741136.1:n.1191A>C
XR_001741137.1:n.1191A>C
XR_001741138.1:n.1191A>C
XR_001741139.1:n.1186A>C