Canonical Allele Identifier: CA358374594
Gene: PABPC4L HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134200383A>C , CM000666.2:g.134200383A>C GRCh38
NC_000004.11:g.135121538A>C , CM000666.1:g.135121538A>C GRCh37
NC_000004.10:g.135340988A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000421491.4:c.637T>G MANE Select ENSP00000463233.1:p.Tyr213Asp
ENST00000421491.3:c.637T>G ENSP00000463233.1:p.Tyr213Asp
NM_001114734.1:c.811T>G NP_001108206.2:p.Tyr271Asp
NM_001114734.2:c.637T>G MANE Select NP_001108206.3:p.Tyr213Asp
NM_001363585.1:c.637T>G NP_001350514.1:p.Tyr213Asp
XR_001741133.1:n.1176T>G
XR_001741134.1:n.1176T>G
XR_001741135.1:n.1176T>G
XR_001741136.1:n.1176T>G
XR_001741137.1:n.1176T>G
XR_001741138.1:n.1176T>G
XR_001741139.1:n.1171T>G