Canonical Allele Identifier: CA1495815211
Gene: PABPC4L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134200880G= , CM000666.2:g.134200880G= GRCh38
NC_000004.11:g.135122035G= , CM000666.1:g.135122035G= GRCh37
NC_000004.10:g.135341485G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000421491.4:c.140C= MANE Select ENSP00000463233.1:p.Thr47=
ENST00000421491.3:c.140C= ENSP00000463233.1:p.Thr47=
NM_001114734.1:c.314C= NP_001108206.2:p.Thr105=
NM_001114734.2:c.140C= MANE Select NP_001108206.3:p.Thr47=
NM_001363585.1:c.140C= NP_001350514.1:p.Thr47=
XR_001741133.1:n.679C=
XR_001741134.1:n.679C=
XR_001741135.1:n.679C=
XR_001741136.1:n.679C=
XR_001741137.1:n.679C=
XR_001741138.1:n.679C=
XR_001741139.1:n.674C=