Canonical Allele Identifier: CA1495814423

Gene: PABPC4L

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.134200351T= , CM000666.2:g.134200351T=	GRCh38
NC_000004.11:g.135121506T= , CM000666.1:g.135121506T=	GRCh37
NC_000004.10:g.135340956T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421491.4:c.669A= MANE Select	ENSP00000463233.1:p.Thr223=
ENST00000421491.3:c.669A=	ENSP00000463233.1:p.Thr223=
NM_001114734.1:c.843A=	NP_001108206.2:p.Thr281=
NM_001114734.2:c.669A= MANE Select	NP_001108206.3:p.Thr223=
NM_001363585.1:c.669A=	NP_001350514.1:p.Thr223=
XR_001741133.1:n.1208A=
XR_001741134.1:n.1208A=
XR_001741135.1:n.1208A=
XR_001741136.1:n.1208A=
XR_001741137.1:n.1208A=
XR_001741138.1:n.1208A=
XR_001741139.1:n.1203A=