Canonical Allele Identifier: CA1188035061
Gene: CELSR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109264401_109264402delinsCA , CM000663.2:g.109264401_109264402delinsCA GRCh38
NC_000001.10:g.109807023_109807024delinsCA , CM000663.1:g.109807023_109807024delinsCA GRCh37
NC_000001.9:g.109608546_109608547delinsCA NCBI36
NG_052669.1:g.19697_19698delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000271332.4:c.5289+36_5289+37delinsCA MANE Select ENSP00000271332.3:n.5289+36_5289+37delinsCA
ENST00000271332.3:c.5289+36_5289+37delinsCA ENSP00000271332.3:n.5289+36_5289+37delinsCA
NM_001408.2:c.5289+36_5289+37delinsCA NP_001399.1:n.5289+36_5289+37delinsCA
XM_005270580.3:c.5289+36_5289+37delinsCA XP_005270637.1:n.5289+36_5289+37delinsCA
NM_001408.3:c.5289+36_5289+37delinsCA MANE Select NP_001399.1:n.5289+36_5289+37delinsCA