Canonical Allele Identifier: CA572109215
Gene: UNCX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.1234109_1234110insCCCCC , CM000669.2:g.1234109_1234110insCCCCC GRCh38
NC_000007.13:g.1273745_1273746insCCCCC , CM000669.1:g.1273745_1273746insCCCCC GRCh37
NC_000007.12:g.1240271_1240272insCCCCC NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000316333.9:c.450+414_450+415insCCCCC MANE Select ENSP00000314480.8:n.450+414_450+415insCCC...
ENST00000316333.8:c.450+414_450+415insCCCCC ENSP00000314480.8:n.450+414_450+415insCCC...
NM_001080461.1:c.450+414_450+415insCCCCC NP_001073930.1:n.450+414_450+415insCCCCC
NM_001080461.2:c.450+414_450+415insCCCCC NP_001073930.1:n.450+414_450+415insCCCCC
NM_001080461.3:c.450+414_450+415insCCCCC MANE Select NP_001073930.1:n.450+414_450+415insCCCCC