Canonical Allele Identifier: CA1188035097
Gene: CELSR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109264463G= , CM000663.2:g.109264463G= GRCh38
NC_000001.10:g.109807085G= , CM000663.1:g.109807085G= GRCh37
NC_000001.9:g.109608608G= NCBI36
NG_052669.1:g.19759G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000271332.4:c.5299G= MANE Select ENSP00000271332.3:p.Val1767=
ENST00000271332.3:c.5299G= ENSP00000271332.3:p.Val1767=
NM_001408.2:c.5299G= NP_001399.1:p.Val1767=
XM_005270580.3:c.5299G= XP_005270637.1:p.Val1767=
NM_001408.3:c.5299G= MANE Select NP_001399.1:p.Val1767=