Canonical Allele Identifier: CA1188034903
Gene: CELSR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109264027_109264028delinsAC , CM000663.2:g.109264027_109264028delinsAC GRCh38
NC_000001.10:g.109806649_109806650delinsAC , CM000663.1:g.109806649_109806650delinsAC GRCh37
NC_000001.9:g.109608172_109608173delinsAC NCBI36
NG_052669.1:g.19323_19324delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000271332.4:c.5002-51_5002-50delinsAC MANE Select ENSP00000271332.3:n.5002-51_5002-50delinsAC
ENST00000271332.3:c.5002-51_5002-50delinsAC ENSP00000271332.3:n.5002-51_5002-50delinsAC
NM_001408.2:c.5002-51_5002-50delinsAC NP_001399.1:n.5002-51_5002-50delinsAC
XM_005270580.3:c.5002-51_5002-50delinsAC XP_005270637.1:n.5002-51_5002-50delinsAC
NM_001408.3:c.5002-51_5002-50delinsAC MANE Select NP_001399.1:n.5002-51_5002-50delinsAC