Canonical Allele Identifier: CA1495814522

Gene: PABPC4L

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.134200419T= , CM000666.2:g.134200419T=	GRCh38
NC_000004.11:g.135121574T= , CM000666.1:g.135121574T=	GRCh37
NC_000004.10:g.135341024T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421491.4:c.601A= MANE Select	ENSP00000463233.1:p.Met201=
ENST00000421491.3:c.601A=	ENSP00000463233.1:p.Met201=
NM_001114734.1:c.775A=	NP_001108206.2:p.Met259=
NM_001114734.2:c.601A= MANE Select	NP_001108206.3:p.Met201=
NM_001363585.1:c.601A=	NP_001350514.1:p.Met201=
XR_001741133.1:n.1140A=
XR_001741134.1:n.1140A=
XR_001741135.1:n.1140A=
XR_001741136.1:n.1140A=
XR_001741137.1:n.1140A=
XR_001741138.1:n.1140A=
XR_001741139.1:n.1135A=