Canonical Allele Identifier: CA441362137

Gene: PABPC4L

Linked Data

• MyVariant Identifiers: chr4:g.135122046C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.134200891C>T , CM000666.2:g.134200891C>T	GRCh38
NC_000004.11:g.135122046C>T , CM000666.1:g.135122046C>T	GRCh37
NC_000004.10:g.135341496C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421491.4:c.129G>A MANE Select	ENSP00000463233.1:p.Arg43=
ENST00000421491.3:c.129G>A	ENSP00000463233.1:p.Arg43=
NM_001114734.1:c.303G>A	NP_001108206.2:p.Arg101=
NM_001114734.2:c.129G>A MANE Select	NP_001108206.3:p.Arg43=
NM_001363585.1:c.129G>A	NP_001350514.1:p.Arg43=
XR_001741133.1:n.668G>A
XR_001741134.1:n.668G>A
XR_001741135.1:n.668G>A
XR_001741136.1:n.668G>A
XR_001741137.1:n.668G>A
XR_001741138.1:n.668G>A
XR_001741139.1:n.663G>A