Canonical Allele Identifier: CA1495815033
Gene: PABPC4L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134200771G= , CM000666.2:g.134200771G= GRCh38
NC_000004.11:g.135121926G= , CM000666.1:g.135121926G= GRCh37
NC_000004.10:g.135341376G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000421491.4:c.249C= MANE Select ENSP00000463233.1:p.Leu83=
ENST00000421491.3:c.249C= ENSP00000463233.1:p.Leu83=
NM_001114734.1:c.423C= NP_001108206.2:p.Leu141=
NM_001114734.2:c.249C= MANE Select NP_001108206.3:p.Leu83=
NM_001363585.1:c.249C= NP_001350514.1:p.Leu83=
XR_001741133.1:n.788C=
XR_001741134.1:n.788C=
XR_001741135.1:n.788C=
XR_001741136.1:n.788C=
XR_001741137.1:n.788C=
XR_001741138.1:n.788C=
XR_001741139.1:n.783C=