Canonical Allele Identifier: CA358374590
Gene: PABPC4L HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134200381A>T , CM000666.2:g.134200381A>T GRCh38
NC_000004.11:g.135121536A>T , CM000666.1:g.135121536A>T GRCh37
NC_000004.10:g.135340986A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000421491.4:c.639T>A MANE Select ENSP00000463233.1:p.Tyr213Ter
ENST00000421491.3:c.639T>A ENSP00000463233.1:p.Tyr213Ter
NM_001114734.1:c.813T>A NP_001108206.2:p.Tyr271Ter
NM_001114734.2:c.639T>A MANE Select NP_001108206.3:p.Tyr213Ter
NM_001363585.1:c.639T>A NP_001350514.1:p.Tyr213Ter
XR_001741133.1:n.1178T>A
XR_001741134.1:n.1178T>A
XR_001741135.1:n.1178T>A
XR_001741136.1:n.1178T>A
XR_001741137.1:n.1178T>A
XR_001741138.1:n.1178T>A
XR_001741139.1:n.1173T>A