Canonical Allele Identifier: CA358374553
Gene: PABPC4L HGNC NCBI

Linked Data

gnomAD v4: 4-134200364-A-G
MyVariant Identifiers: chr4:g.135121519A>G (hg19) chr4:g.134200364A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134200364A>G , CM000666.2:g.134200364A>G GRCh38
NC_000004.11:g.135121519A>G , CM000666.1:g.135121519A>G GRCh37
NC_000004.10:g.135340969A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000421491.4:c.656T>C MANE Select ENSP00000463233.1:p.Val219Ala
ENST00000421491.3:c.656T>C ENSP00000463233.1:p.Val219Ala
NM_001114734.1:c.830T>C NP_001108206.2:p.Val277Ala
NM_001114734.2:c.656T>C MANE Select NP_001108206.3:p.Val219Ala
NM_001363585.1:c.656T>C NP_001350514.1:p.Val219Ala
XR_001741133.1:n.1195T>C
XR_001741134.1:n.1195T>C
XR_001741135.1:n.1195T>C
XR_001741136.1:n.1195T>C
XR_001741137.1:n.1195T>C
XR_001741138.1:n.1195T>C
XR_001741139.1:n.1190T>C
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