Canonical Allele Identifier: CA1495814699
Gene: PABPC4L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134200547T= , CM000666.2:g.134200547T= GRCh38
NC_000004.11:g.135121702T= , CM000666.1:g.135121702T= GRCh37
NC_000004.10:g.135341152T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000421491.4:c.473A= MANE Select ENSP00000463233.1:p.Asn158=
ENST00000421491.3:c.473A= ENSP00000463233.1:p.Asn158=
NM_001114734.1:c.647A= NP_001108206.2:p.Asn216=
NM_001114734.2:c.473A= MANE Select NP_001108206.3:p.Asn158=
NM_001363585.1:c.473A= NP_001350514.1:p.Asn158=
XR_001741133.1:n.1012A=
XR_001741134.1:n.1012A=
XR_001741135.1:n.1012A=
XR_001741136.1:n.1012A=
XR_001741137.1:n.1012A=
XR_001741138.1:n.1012A=
XR_001741139.1:n.1007A=