Canonical Allele Identifier: CA15069764

Gene: PABPC4

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39562508A>G , CM000663.2:g.39562508A>G	GRCh38
NC_000001.10:g.40028180A>G , CM000663.1:g.40028180A>G	GRCh37
NC_000001.9:g.39800767A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372858.8:c.1669-92T>C MANE Select	ENSP00000361949.3:n.1669-92T>C
ENST00000470443.6:c.1549-92T>C
ENST00000527718.2:c.797-92T>C
ENST00000676523.1:n.2236-92T>C
ENST00000676859.1:c.751-92T>C	ENSP00000504204.1:n.751-92T>C
ENST00000676863.1:n.3047T>C
ENST00000677006.1:c.1483-92T>C	ENSP00000504742.1:n.1483-92T>C
ENST00000677244.1:n.2793T>C
ENST00000677548.1:n.6639T>C
ENST00000677609.1:c.1492-92T>C	ENSP00000504105.1:n.1492-92T>C
ENST00000677708.1:n.652-92T>C
ENST00000677860.1:n.1424-92T>C
ENST00000678028.1:n.377-92T>C
ENST00000678287.1:n.2459-92T>C
ENST00000678469.1:c.494-92T>C
ENST00000678625.1:c.1441-92T>C	ENSP00000504391.1:n.1441-92T>C
ENST00000678894.1:n.3890T>C
ENST00000678980.1:n.2841T>C
ENST00000679246.1:n.2553-92T>C
ENST00000372856.7:c.1582-92T>C	ENSP00000361947.3:n.1582-92T>C
ENST00000372857.7:c.1621-92T>C	ENSP00000361948.3:n.1621-92T>C
ENST00000372858.7:c.1669-92T>C	ENSP00000361949.3:n.1669-92T>C
ENST00000372862.7:c.1534-92T>C	ENSP00000361953.3:n.1534-92T>C
ENST00000421687.6:c.1374-128T>C
ENST00000437136.5:c.285-92T>C
ENST00000468476.1:n.2019T>C
ENST00000484555.1:n.418-92T>C
ENST00000492468.5:n.1531T>C
NM_001135653.1:c.1669-92T>C	NP_001129125.1:n.1669-92T>C
NM_001135654.1:c.1582-92T>C	NP_001129126.1:n.1582-92T>C
NM_003819.3:c.1621-92T>C	NP_003810.1:n.1621-92T>C
NM_001135653.2:c.1669-92T>C MANE Select	NP_001129125.1:n.1669-92T>C
NM_001135654.2:c.1582-92T>C	NP_001129126.1:n.1582-92T>C
NM_003819.4:c.1621-92T>C	NP_003810.1:n.1621-92T>C