Canonical Allele Identifier: CA358374790
Gene: PABPC4L HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.135121619C>T (hg19) chr4:g.134200464C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134200464C>T , CM000666.2:g.134200464C>T GRCh38
NC_000004.11:g.135121619C>T , CM000666.1:g.135121619C>T GRCh37
NC_000004.10:g.135341069C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000421491.4:c.556G>A MANE Select ENSP00000463233.1:p.Ala186Thr
ENST00000421491.3:c.556G>A ENSP00000463233.1:p.Ala186Thr
NM_001114734.1:c.730G>A NP_001108206.2:p.Ala244Thr
NM_001114734.2:c.556G>A MANE Select NP_001108206.3:p.Ala186Thr
NM_001363585.1:c.556G>A NP_001350514.1:p.Ala186Thr
XR_001741133.1:n.1095G>A
XR_001741134.1:n.1095G>A
XR_001741135.1:n.1095G>A
XR_001741136.1:n.1095G>A
XR_001741137.1:n.1095G>A
XR_001741138.1:n.1095G>A
XR_001741139.1:n.1090G>A
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