Canonical Allele Identifier: CA1682451457

Gene: UNCX

Linked Data

• dbSNP Id: rs1778692517

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.1233949_1233951del , CM000669.2:g.1233949_1233951del	GRCh38
NC_000007.13:g.1273585_1273587del , CM000669.1:g.1273585_1273587del	GRCh37
NC_000007.12:g.1240111_1240113del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316333.9:c.450+254_450+256del MANE Select	ENSP00000314480.8:n.450+254_450+256del
ENST00000316333.8:c.450+254_450+256del	ENSP00000314480.8:n.450+254_450+256del
NM_001080461.1:c.450+254_450+256del	NP_001073930.1:n.450+254_450+256del
NM_001080461.2:c.450+254_450+256del	NP_001073930.1:n.450+254_450+256del
NM_001080461.3:c.450+254_450+256del MANE Select	NP_001073930.1:n.450+254_450+256del