Canonical Allele Identifier: CA358374474

Gene: PABPC4L

Linked Data

• dbSNP Id: rs1578885231
• gnomAD v4: 4-134200328-C-A
• MyVariant Identifiers: chr4:g.135121483C>A (hg19) ; chr4:g.134200328C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.134200328C>A , CM000666.2:g.134200328C>A	GRCh38
NC_000004.11:g.135121483C>A , CM000666.1:g.135121483C>A	GRCh37
NC_000004.10:g.135340933C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421491.4:c.692G>T MANE Select	ENSP00000463233.1:p.Gly231Val
ENST00000421491.3:c.692G>T	ENSP00000463233.1:p.Gly231Val
NM_001114734.1:c.866G>T	NP_001108206.2:p.Gly289Val
NM_001114734.2:c.692G>T MANE Select	NP_001108206.3:p.Gly231Val
NM_001363585.1:c.692G>T	NP_001350514.1:p.Gly231Val
XR_001741133.1:n.1231G>T
XR_001741134.1:n.1231G>T
XR_001741135.1:n.1231G>T
XR_001741136.1:n.1231G>T
XR_001741137.1:n.1231G>T
XR_001741138.1:n.1231G>T
XR_001741139.1:n.1226G>T