Canonical Allele Identifier: CA1140102179
Gene: CELSR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109264477G= , CM000663.2:g.109264477G= GRCh38
NC_000001.10:g.109807099G= , CM000663.1:g.109807099G= GRCh37
NC_000001.9:g.109608622G= NCBI36
NG_052669.1:g.19773G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000271332.4:c.5313G= MANE Select ENSP00000271332.3:p.Pro1771=
ENST00000271332.3:c.5313G= ENSP00000271332.3:p.Pro1771=
NM_001408.2:c.5313G= NP_001399.1:p.Pro1771=
XM_005270580.3:c.5313G= XP_005270637.1:p.Pro1771=
NM_001408.3:c.5313G= MANE Select NP_001399.1:p.Pro1771=