Canonical Allele Identifier: CA358374999
Gene: PABPC4L HGNC NCBI

Linked Data

dbSNP Id: rs1578885605
gnomAD v4: 4-134200556-T-C
MyVariant Identifiers: chr4:g.135121711T>C (hg19) chr4:g.134200556T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134200556T>C , CM000666.2:g.134200556T>C GRCh38
NC_000004.11:g.135121711T>C , CM000666.1:g.135121711T>C GRCh37
NC_000004.10:g.135341161T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000421491.4:c.464A>G MANE Select ENSP00000463233.1:p.Glu155Gly
ENST00000421491.3:c.464A>G ENSP00000463233.1:p.Glu155Gly
NM_001114734.1:c.638A>G NP_001108206.2:p.Glu213Gly
NM_001114734.2:c.464A>G MANE Select NP_001108206.3:p.Glu155Gly
NM_001363585.1:c.464A>G NP_001350514.1:p.Glu155Gly
XR_001741133.1:n.1003A>G
XR_001741134.1:n.1003A>G
XR_001741135.1:n.1003A>G
XR_001741136.1:n.1003A>G
XR_001741137.1:n.1003A>G
XR_001741138.1:n.1003A>G
XR_001741139.1:n.998A>G
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