Canonical Allele Identifier: CA1495814620
Gene: PABPC4L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134200495T= , CM000666.2:g.134200495T= GRCh38
NC_000004.11:g.135121650T= , CM000666.1:g.135121650T= GRCh37
NC_000004.10:g.135341100T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000421491.4:c.525A= MANE Select ENSP00000463233.1:p.Arg175=
ENST00000421491.3:c.525A= ENSP00000463233.1:p.Arg175=
NM_001114734.1:c.699A= NP_001108206.2:p.Arg233=
NM_001114734.2:c.525A= MANE Select NP_001108206.3:p.Arg175=
NM_001363585.1:c.525A= NP_001350514.1:p.Arg175=
XR_001741133.1:n.1064A=
XR_001741134.1:n.1064A=
XR_001741135.1:n.1064A=
XR_001741136.1:n.1064A=
XR_001741137.1:n.1064A=
XR_001741138.1:n.1064A=
XR_001741139.1:n.1059A=