Canonical Allele Identifier: CA358375729
Gene: PABPC4L HGNC NCBI

Linked Data

gnomAD v4: 4-134200880-G-C
MyVariant Identifiers: chr4:g.135122035G>C (hg19) chr4:g.134200880G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134200880G>C , CM000666.2:g.134200880G>C GRCh38
NC_000004.11:g.135122035G>C , CM000666.1:g.135122035G>C GRCh37
NC_000004.10:g.135341485G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000421491.4:c.140C>G MANE Select ENSP00000463233.1:p.Thr47Ser
ENST00000421491.3:c.140C>G ENSP00000463233.1:p.Thr47Ser
NM_001114734.1:c.314C>G NP_001108206.2:p.Thr105Ser
NM_001114734.2:c.140C>G MANE Select NP_001108206.3:p.Thr47Ser
NM_001363585.1:c.140C>G NP_001350514.1:p.Thr47Ser
XR_001741133.1:n.679C>G
XR_001741134.1:n.679C>G
XR_001741135.1:n.679C>G
XR_001741136.1:n.679C>G
XR_001741137.1:n.679C>G
XR_001741138.1:n.679C>G
XR_001741139.1:n.674C>G
Search 100 bp 5'
Search 100 bp 3'