Canonical Allele Identifier: CA1495814489
Gene: PABPC4L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134200405T= , CM000666.2:g.134200405T= GRCh38
NC_000004.11:g.135121560T= , CM000666.1:g.135121560T= GRCh37
NC_000004.10:g.135341010T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000421491.4:c.615A= MANE Select ENSP00000463233.1:p.Arg205=
ENST00000421491.3:c.615A= ENSP00000463233.1:p.Arg205=
NM_001114734.1:c.789A= NP_001108206.2:p.Arg263=
NM_001114734.2:c.615A= MANE Select NP_001108206.3:p.Arg205=
NM_001363585.1:c.615A= NP_001350514.1:p.Arg205=
XR_001741133.1:n.1154A=
XR_001741134.1:n.1154A=
XR_001741135.1:n.1154A=
XR_001741136.1:n.1154A=
XR_001741137.1:n.1154A=
XR_001741138.1:n.1154A=
XR_001741139.1:n.1149A=