Canonical Allele Identifier: CA1188035128
Gene: CELSR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109264547G= , CM000663.2:g.109264547G= GRCh38
NC_000001.10:g.109807169G= , CM000663.1:g.109807169G= GRCh37
NC_000001.9:g.109608692G= NCBI36
NG_052669.1:g.19843G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000271332.4:c.5383G= MANE Select ENSP00000271332.3:p.Asp1795=
ENST00000271332.3:c.5383G= ENSP00000271332.3:p.Asp1795=
NM_001408.2:c.5383G= NP_001399.1:p.Asp1795=
XM_005270580.3:c.5383G= XP_005270637.1:p.Asp1795=
NM_001408.3:c.5383G= MANE Select NP_001399.1:p.Asp1795=