Canonical Allele Identifier: CA1188035072
Gene: CELSR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109264414_109264417delinsCCCG , CM000663.2:g.109264414_109264417delinsCCCG GRCh38
NC_000001.10:g.109807036_109807039delinsCCCG , CM000663.1:g.109807036_109807039delinsCCCG GRCh37
NC_000001.9:g.109608559_109608562delinsCCCG NCBI36
NG_052669.1:g.19710_19713delinsCCCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000271332.4:c.5290-40_5290-37delinsCCCG MANE Select ENSP00000271332.3:n.5290-40_5290-37delinsCCCG
ENST00000271332.3:c.5290-40_5290-37delinsCCCG ENSP00000271332.3:n.5290-40_5290-37delinsCCCG
NM_001408.2:c.5290-40_5290-37delinsCCCG NP_001399.1:n.5290-40_5290-37delinsCCCG
XM_005270580.3:c.5290-40_5290-37delinsCCCG XP_005270637.1:n.5290-40_5290-37delinsCCCG
NM_001408.3:c.5290-40_5290-37delinsCCCG MANE Select NP_001399.1:n.5290-40_5290-37delinsCCCG