Canonical Allele Identifier: CA358374454
Gene: PABPC4L HGNC NCBI

Linked Data

dbSNP Id: rs1335600013

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134200319A>T , CM000666.2:g.134200319A>T GRCh38
NC_000004.11:g.135121474A>T , CM000666.1:g.135121474A>T GRCh37
NC_000004.10:g.135340924A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000421491.4:c.701T>A MANE Select ENSP00000463233.1:p.Phe234Tyr
ENST00000421491.3:c.701T>A ENSP00000463233.1:p.Phe234Tyr
NM_001114734.1:c.875T>A NP_001108206.2:p.Phe292Tyr
NM_001114734.2:c.701T>A MANE Select NP_001108206.3:p.Phe234Tyr
NM_001363585.1:c.701T>A NP_001350514.1:p.Phe234Tyr
XR_001741133.1:n.1240T>A
XR_001741134.1:n.1240T>A
XR_001741135.1:n.1240T>A
XR_001741136.1:n.1240T>A
XR_001741137.1:n.1240T>A
XR_001741138.1:n.1240T>A
XR_001741139.1:n.1235T>A