Canonical Allele Identifier: CA766794363

Gene: UBXN2A

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.23931322A>G , CM000664.2:g.23931322A>G	GRCh38
NC_000002.11:g.24154192A>G , CM000664.1:g.24154192A>G	GRCh37
NC_000002.10:g.24007696A>G	NCBI36
NG_029017.2:g.745T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404924.5:c.-138+3707A>G	ENSP00000385525.1:n.-138+3707A>G
ENST00000446425.2:n.331+3707A>G
XM_005264166.3:c.-15+3707A>G	XP_005264223.1:n.-15+3707A>G
XM_011532632.1:c.-148+3707A>G	XP_011530934.1:n.-148+3707A>G
XM_011532633.1:c.-138+3707A>G	XP_011530935.1:n.-138+3707A>G
XM_005264166.5:c.-15+3707A>G	XP_005264223.1:n.-15+3707A>G
XM_005264168.5:c.-152+3707A>G	XP_005264225.1:n.-152+3707A>G
XM_011532633.3:c.-138+3707A>G	XP_011530935.1:n.-138+3707A>G
XM_024452738.1:c.-53+3707A>G	XP_024308506.1:n.-53+3707A>G