Canonical Allele Identifier: CA1188031645
Gene: CELSR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109274578C= , CM000663.2:g.109274578C= GRCh38
NC_000001.10:g.109817200C= , CM000663.1:g.109817200C= GRCh37
NC_000001.9:g.109618723C= NCBI36
NG_052669.1:g.29874C=

Transcript Alleles

HGVS Amino-acid change
ENST00000271332.4:c.*529C= MANE Select ENSP00000271332.3:n.*529C=
ENST00000271332.3:c.*529C= ENSP00000271332.3:n.*529C=
ENST00000498157.1:n.2651C=
NM_001408.2:c.*529C= NP_001399.1:n.*529C=
XM_005270580.3:c.*396C= XP_005270637.1:n.*396C=
NM_001408.3:c.*529C= MANE Select NP_001399.1:n.*529C=