Canonical Allele Identifier: CA358375629
Gene: PABPC4L HGNC NCBI

Linked Data

dbSNP Id: rs1729843514

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134200832T>C , CM000666.2:g.134200832T>C GRCh38
NC_000004.11:g.135121987T>C , CM000666.1:g.135121987T>C GRCh37
NC_000004.10:g.135341437T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000421491.4:c.188A>G MANE Select ENSP00000463233.1:p.Asp63Gly
ENST00000421491.3:c.188A>G ENSP00000463233.1:p.Asp63Gly
NM_001114734.1:c.362A>G NP_001108206.2:p.Asp121Gly
NM_001114734.2:c.188A>G MANE Select NP_001108206.3:p.Asp63Gly
NM_001363585.1:c.188A>G NP_001350514.1:p.Asp63Gly
XR_001741133.1:n.727A>G
XR_001741134.1:n.727A>G
XR_001741135.1:n.727A>G
XR_001741136.1:n.727A>G
XR_001741137.1:n.727A>G
XR_001741138.1:n.727A>G
XR_001741139.1:n.722A>G