Canonical Allele Identifier: CA358374528

Gene: PABPC4L

Linked Data

• MyVariant Identifiers: chr4:g.135121507G>T (hg19) ; chr4:g.134200352G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.134200352G>T , CM000666.2:g.134200352G>T	GRCh38
NC_000004.11:g.135121507G>T , CM000666.1:g.135121507G>T	GRCh37
NC_000004.10:g.135340957G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421491.4:c.668C>A MANE Select	ENSP00000463233.1:p.Thr223Lys
ENST00000421491.3:c.668C>A	ENSP00000463233.1:p.Thr223Lys
NM_001114734.1:c.842C>A	NP_001108206.2:p.Thr281Lys
NM_001114734.2:c.668C>A MANE Select	NP_001108206.3:p.Thr223Lys
NM_001363585.1:c.668C>A	NP_001350514.1:p.Thr223Lys
XR_001741133.1:n.1207C>A
XR_001741134.1:n.1207C>A
XR_001741135.1:n.1207C>A
XR_001741136.1:n.1207C>A
XR_001741137.1:n.1207C>A
XR_001741138.1:n.1207C>A
XR_001741139.1:n.1202C>A