Canonical Allele Identifier: CA358374941
Gene: PABPC4L HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134200530C>T , CM000666.2:g.134200530C>T GRCh38
NC_000004.11:g.135121685C>T , CM000666.1:g.135121685C>T GRCh37
NC_000004.10:g.135341135C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000421491.4:c.490G>A MANE Select ENSP00000463233.1:p.Gly164Ser
ENST00000421491.3:c.490G>A ENSP00000463233.1:p.Gly164Ser
NM_001114734.1:c.664G>A NP_001108206.2:p.Gly222Ser
NM_001114734.2:c.490G>A MANE Select NP_001108206.3:p.Gly164Ser
NM_001363585.1:c.490G>A NP_001350514.1:p.Gly164Ser
XR_001741133.1:n.1029G>A
XR_001741134.1:n.1029G>A
XR_001741135.1:n.1029G>A
XR_001741136.1:n.1029G>A
XR_001741137.1:n.1029G>A
XR_001741138.1:n.1029G>A
XR_001741139.1:n.1024G>A