Canonical Allele Identifier: CA1188034919
Gene: CELSR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109264055G= , CM000663.2:g.109264055G= GRCh38
NC_000001.10:g.109806677G= , CM000663.1:g.109806677G= GRCh37
NC_000001.9:g.109608200G= NCBI36
NG_052669.1:g.19351G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000271332.4:c.5002-23G= MANE Select ENSP00000271332.3:n.5002-23G=
ENST00000271332.3:c.5002-23G= ENSP00000271332.3:n.5002-23G=
NM_001408.2:c.5002-23G= NP_001399.1:n.5002-23G=
XM_005270580.3:c.5002-23G= XP_005270637.1:n.5002-23G=
NM_001408.3:c.5002-23G= MANE Select NP_001399.1:n.5002-23G=