Canonical Allele Identifier: CA1495815170
Gene: PABPC4L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134200859G= , CM000666.2:g.134200859G= GRCh38
NC_000004.11:g.135122014G= , CM000666.1:g.135122014G= GRCh37
NC_000004.10:g.135341464G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000421491.4:c.161C= MANE Select ENSP00000463233.1:p.Ala54=
ENST00000421491.3:c.161C= ENSP00000463233.1:p.Ala54=
NM_001114734.1:c.335C= NP_001108206.2:p.Ala112=
NM_001114734.2:c.161C= MANE Select NP_001108206.3:p.Ala54=
NM_001363585.1:c.161C= NP_001350514.1:p.Ala54=
XR_001741133.1:n.700C=
XR_001741134.1:n.700C=
XR_001741135.1:n.700C=
XR_001741136.1:n.700C=
XR_001741137.1:n.700C=
XR_001741138.1:n.700C=
XR_001741139.1:n.695C=