Canonical Allele Identifier: CA1140636028
Gene: CELSR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109263928G= , CM000663.2:g.109263928G= GRCh38
NC_000001.10:g.109806550G= , CM000663.1:g.109806550G= GRCh37
NC_000001.9:g.109608073G= NCBI36
NG_052669.1:g.19224G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000271332.4:c.5002-150G= MANE Select ENSP00000271332.3:n.5002-150G=
ENST00000271332.3:c.5002-150G= ENSP00000271332.3:n.5002-150G=
NM_001408.2:c.5002-150G= NP_001399.1:n.5002-150G=
XM_005270580.3:c.5002-150G= XP_005270637.1:n.5002-150G=
NM_001408.3:c.5002-150G= MANE Select NP_001399.1:n.5002-150G=