Canonical Allele Identifier: CA1188031647
Gene: CELSR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109274580C= , CM000663.2:g.109274580C= GRCh38
NC_000001.10:g.109817202C= , CM000663.1:g.109817202C= GRCh37
NC_000001.9:g.109618725C= NCBI36
NG_052669.1:g.29876C=

Transcript Alleles

HGVS Amino-acid change
ENST00000271332.4:c.*531C= MANE Select ENSP00000271332.3:n.*531C=
ENST00000271332.3:c.*531C= ENSP00000271332.3:n.*531C=
ENST00000498157.1:n.2653C=
NM_001408.2:c.*531C= NP_001399.1:n.*531C=
XM_005270580.3:c.*398C= XP_005270637.1:n.*398C=
NM_001408.3:c.*531C= MANE Select NP_001399.1:n.*531C=