Canonical Allele Identifier: CA358374466
Gene: PABPC4L HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.135121480A>C (hg19) chr4:g.134200325A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134200325A>C , CM000666.2:g.134200325A>C GRCh38
NC_000004.11:g.135121480A>C , CM000666.1:g.135121480A>C GRCh37
NC_000004.10:g.135340930A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000421491.4:c.695T>G MANE Select ENSP00000463233.1:p.Phe232Cys
ENST00000421491.3:c.695T>G ENSP00000463233.1:p.Phe232Cys
NM_001114734.1:c.869T>G NP_001108206.2:p.Phe290Cys
NM_001114734.2:c.695T>G MANE Select NP_001108206.3:p.Phe232Cys
NM_001363585.1:c.695T>G NP_001350514.1:p.Phe232Cys
XR_001741133.1:n.1234T>G
XR_001741134.1:n.1234T>G
XR_001741135.1:n.1234T>G
XR_001741136.1:n.1234T>G
XR_001741137.1:n.1234T>G
XR_001741138.1:n.1234T>G
XR_001741139.1:n.1229T>G
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