Canonical Allele Identifier: CA1682451624

Gene: UNCX

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.1234157_1234158delinsTG , CM000669.2:g.1234157_1234158delinsTG	GRCh38
NC_000007.13:g.1273793_1273794delinsTG , CM000669.1:g.1273793_1273794delinsTG	GRCh37
NC_000007.12:g.1240319_1240320delinsTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316333.9:c.450+462_450+463delinsTG MANE Select	ENSP00000314480.8:n.450+462_450+463delinsTG
ENST00000316333.8:c.450+462_450+463delinsTG	ENSP00000314480.8:n.450+462_450+463delinsTG
NM_001080461.1:c.450+462_450+463delinsTG	NP_001073930.1:n.450+462_450+463delinsTG
NM_001080461.2:c.450+462_450+463delinsTG	NP_001073930.1:n.450+462_450+463delinsTG
NM_001080461.3:c.450+462_450+463delinsTG MANE Select	NP_001073930.1:n.450+462_450+463delinsTG