Canonical Allele Identifier: CA106325861
Gene: PABPC4L HGNC NCBI

Linked Data

dbSNP Id: rs971112138

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000421491.4:c.142dup MANE Select ENSP00000463233.1:p.Arg48ProfsTer16
ENST00000421491.3:c.142dup ENSP00000463233.1:p.Arg48ProfsTer16
NM_001114734.1:c.316dup NP_001108206.2:p.Arg106ProfsTer16
NM_001114734.2:c.142dup MANE Select NP_001108206.3:p.Arg48ProfsTer16
NM_001363585.1:c.142dup NP_001350514.1:p.Arg48ProfsTer16
XR_001741133.1:n.681dup
XR_001741134.1:n.681dup
XR_001741135.1:n.681dup
XR_001741136.1:n.681dup
XR_001741137.1:n.681dup
XR_001741138.1:n.681dup
XR_001741139.1:n.676dup