Canonical Allele Identifier: CA1495814502
Gene: PABPC4L HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134200412T= , CM000666.2:g.134200412T= GRCh38
NC_000004.11:g.135121567T= , CM000666.1:g.135121567T= GRCh37
NC_000004.10:g.135341017T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000421491.4:c.608A= MANE Select ENSP00000463233.1:p.Asp203=
ENST00000421491.3:c.608A= ENSP00000463233.1:p.Asp203=
NM_001114734.1:c.782A= NP_001108206.2:p.Asp261=
NM_001114734.2:c.608A= MANE Select NP_001108206.3:p.Asp203=
NM_001363585.1:c.608A= NP_001350514.1:p.Asp203=
XR_001741133.1:n.1147A=
XR_001741134.1:n.1147A=
XR_001741135.1:n.1147A=
XR_001741136.1:n.1147A=
XR_001741137.1:n.1147A=
XR_001741138.1:n.1147A=
XR_001741139.1:n.1142A=
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