Canonical Allele Identifier: CA1495814349
Gene: PABPC4L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134200296C= , CM000666.2:g.134200296C= GRCh38
NC_000004.11:g.135121451C= , CM000666.1:g.135121451C= GRCh37
NC_000004.10:g.135340901C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000421491.4:c.724G= MANE Select ENSP00000463233.1:p.Ala242=
ENST00000421491.3:c.724G= ENSP00000463233.1:p.Ala242=
NM_001114734.1:c.898G= NP_001108206.2:p.Ala300=
NM_001114734.2:c.724G= MANE Select NP_001108206.3:p.Ala242=
NM_001363585.1:c.724G= NP_001350514.1:p.Ala242=
XR_001741133.1:n.1263G=
XR_001741134.1:n.1263G=
XR_001741135.1:n.1263G=
XR_001741136.1:n.1263G=
XR_001741137.1:n.1263G=
XR_001741138.1:n.1263G=
XR_001741139.1:n.1258G=