Canonical Allele Identifier: CA1495814378
Gene: PABPC4L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134200316A= , CM000666.2:g.134200316A= GRCh38
NC_000004.11:g.135121471A= , CM000666.1:g.135121471A= GRCh37
NC_000004.10:g.135340921A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000421491.4:c.704T= MANE Select ENSP00000463233.1:p.Val235=
ENST00000421491.3:c.704T= ENSP00000463233.1:p.Val235=
NM_001114734.1:c.878T= NP_001108206.2:p.Val293=
NM_001114734.2:c.704T= MANE Select NP_001108206.3:p.Val235=
NM_001363585.1:c.704T= NP_001350514.1:p.Val235=
XR_001741133.1:n.1243T=
XR_001741134.1:n.1243T=
XR_001741135.1:n.1243T=
XR_001741136.1:n.1243T=
XR_001741137.1:n.1243T=
XR_001741138.1:n.1243T=
XR_001741139.1:n.1238T=