Canonical Allele Identifier: CA1890920494

Gene: UPF2

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.12009817G>C , CM000672.2:g.12009817G>C	GRCh38
NC_000010.10:g.12051816G>C , CM000672.1:g.12051816G>C	GRCh37
NC_000010.9:g.12091822G>C	NCBI36
NG_033936.1:g.38354C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357604.10:c.1306+4207C>G MANE Select	ENSP00000350221.5:n.1306+4207C>G
ENST00000356352.6:c.1306+4207C>G	ENSP00000348708.2:n.1306+4207C>G
ENST00000357604.9:c.1306+4207C>G	ENSP00000350221.5:n.1306+4207C>G
ENST00000397053.6:c.1306+4207C>G	ENSP00000380244.2:n.1306+4207C>G
NM_015542.3:c.1306+4207C>G	NP_056357.1:n.1306+4207C>G
NM_080599.2:c.1306+4207C>G	NP_542166.1:n.1306+4207C>G
XM_011519447.1:c.1306+4207C>G	XP_011517749.1:n.1306+4207C>G
XM_011519448.1:c.1306+4207C>G	XP_011517750.1:n.1306+4207C>G
XM_011519449.1:c.1306+4207C>G	XP_011517751.1:n.1306+4207C>G
XR_930489.1:n.1379+4207C>G
XM_011519449.3:c.1306+4207C>G	XP_011517751.1:n.1306+4207C>G
XR_930489.3:n.1411+4207C>G
NM_015542.4:c.1306+4207C>G MANE Select	NP_056357.1:n.1306+4207C>G
NM_080599.3:c.1306+4207C>G	NP_542166.1:n.1306+4207C>G