Canonical Allele Identifier: CA1188034927
Gene: CELSR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109264072T= , CM000663.2:g.109264072T= GRCh38
NC_000001.10:g.109806694T= , CM000663.1:g.109806694T= GRCh37
NC_000001.9:g.109608217T= NCBI36
NG_052669.1:g.19368T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000271332.4:c.5002-6T= MANE Select ENSP00000271332.3:n.5002-6T=
ENST00000271332.3:c.5002-6T= ENSP00000271332.3:n.5002-6T=
NM_001408.2:c.5002-6T= NP_001399.1:n.5002-6T=
XM_005270580.3:c.5002-6T= XP_005270637.1:n.5002-6T=
NM_001408.3:c.5002-6T= MANE Select NP_001399.1:n.5002-6T=