Canonical Allele Identifier: CA1682451456

Gene: UNCX

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.1233946_1233949delinsAGCG , CM000669.2:g.1233946_1233949delinsAGCG	GRCh38
NC_000007.13:g.1273582_1273585delinsAGCG , CM000669.1:g.1273582_1273585delinsAGCG	GRCh37
NC_000007.12:g.1240108_1240111delinsAGCG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316333.9:c.450+251_450+254delinsAGCG MANE Select	ENSP00000314480.8:n.450+251_450+254delinsAGCG
ENST00000316333.8:c.450+251_450+254delinsAGCG	ENSP00000314480.8:n.450+251_450+254delinsAGCG
NM_001080461.1:c.450+251_450+254delinsAGCG	NP_001073930.1:n.450+251_450+254delinsAGCG
NM_001080461.2:c.450+251_450+254delinsAGCG	NP_001073930.1:n.450+251_450+254delinsAGCG
NM_001080461.3:c.450+251_450+254delinsAGCG MANE Select	NP_001073930.1:n.450+251_450+254delinsAGCG