Canonical Allele Identifier: CA2744995064
Gene: CELSR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109264390_109264391insCCCCCCCCCCCCCCCCCCC , CM000663.2:g.109264390_109264391insCCCCCCCCCCCCCCCCCCC GRCh38
NC_000001.10:g.109807012_109807013insCCCCCCCCCCCCCCCCCCC , CM000663.1:g.109807012_109807013insCCCCCCCCCCCCCCCCCCC GRCh37
NC_000001.9:g.109608535_109608536insCCCCCCCCCCCCCCCCCCC NCBI36
NG_052669.1:g.19686_19687insCCCCCCCCCCCCCCCCCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000271332.4:c.5289+25_5289+26insCCCCCCCCCCCCCCCCCCC MANE Select ENSP00000271332.3:n.5289+25_5289+26insCCCCCCCCCCCCCCCCCCC
ENST00000271332.3:c.5289+25_5289+26insCCCCCCCCCCCCCCCCCCC ENSP00000271332.3:n.5289+25_5289+26insCCCCCCCCCCCCCCCCCCC
NM_001408.2:c.5289+25_5289+26insCCCCCCCCCCCCCCCCCCC NP_001399.1:n.5289+25_5289+26insCCCCCCCCCCCCCCCCCCC
XM_005270580.3:c.5289+25_5289+26insCCCCCCCCCCCCCCCCCCC XP_005270637.1:n.5289+25_5289+26insCCCCCCCCCCCCCCCCCCC
NM_001408.3:c.5289+25_5289+26insCCCCCCCCCCCCCCCCCCC MANE Select NP_001399.1:n.5289+25_5289+26insCCCCCCCCCCCCCCCCCCC