Canonical Allele Identifier: CA358375435
Gene: PABPC4L HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.135121900A>T (hg19) chr4:g.134200745A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134200745A>T , CM000666.2:g.134200745A>T GRCh38
NC_000004.11:g.135121900A>T , CM000666.1:g.135121900A>T GRCh37
NC_000004.10:g.135341350A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000421491.4:c.275T>A MANE Select ENSP00000463233.1:p.Leu92Ter
ENST00000421491.3:c.275T>A ENSP00000463233.1:p.Leu92Ter
NM_001114734.1:c.449T>A NP_001108206.2:p.Leu150Ter
NM_001114734.2:c.275T>A MANE Select NP_001108206.3:p.Leu92Ter
NM_001363585.1:c.275T>A NP_001350514.1:p.Leu92Ter
XR_001741133.1:n.814T>A
XR_001741134.1:n.814T>A
XR_001741135.1:n.814T>A
XR_001741136.1:n.814T>A
XR_001741137.1:n.814T>A
XR_001741138.1:n.814T>A
XR_001741139.1:n.809T>A
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