Canonical Allele Identifier: CA1097509658

Gene: UNCX

Linked Data

• dbSNP Id: rs1778695683
• gnomAD v3: 7-1234082-C-CA
• gnomAD v4: 7-1234082-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.1234082_1234083insA , CM000669.2:g.1234082_1234083insA	GRCh38
NC_000007.13:g.1273718_1273719insA , CM000669.1:g.1273718_1273719insA	GRCh37
NC_000007.12:g.1240244_1240245insA	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000316333.9:c.450+387_450+388insA MANE Select	ENSP00000314480.8:n.450+387_450+388insA
ENST00000316333.8:c.450+387_450+388insA	ENSP00000314480.8:n.450+387_450+388insA
NM_001080461.1:c.450+387_450+388insA	NP_001073930.1:n.450+387_450+388insA
NM_001080461.2:c.450+387_450+388insA	NP_001073930.1:n.450+387_450+388insA
NM_001080461.3:c.450+387_450+388insA MANE Select	NP_001073930.1:n.450+387_450+388insA