Canonical Allele Identifier: CA1495815104
Gene: PABPC4L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134200808A= , CM000666.2:g.134200808A= GRCh38
NC_000004.11:g.135121963A= , CM000666.1:g.135121963A= GRCh37
NC_000004.10:g.135341413A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000421491.4:c.212T= MANE Select ENSP00000463233.1:p.Met71=
ENST00000421491.3:c.212T= ENSP00000463233.1:p.Met71=
NM_001114734.1:c.386T= NP_001108206.2:p.Met129=
NM_001114734.2:c.212T= MANE Select NP_001108206.3:p.Met71=
NM_001363585.1:c.212T= NP_001350514.1:p.Met71=
XR_001741133.1:n.751T=
XR_001741134.1:n.751T=
XR_001741135.1:n.751T=
XR_001741136.1:n.751T=
XR_001741137.1:n.751T=
XR_001741138.1:n.751T=
XR_001741139.1:n.746T=