Canonical Allele Identifier: CA1188034931
Gene: CELSR2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109264078C= , CM000663.2:g.109264078C= GRCh38
NC_000001.10:g.109806700C= , CM000663.1:g.109806700C= GRCh37
NC_000001.9:g.109608223C= NCBI36
NG_052669.1:g.19374C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000271332.4:c.5002C= MANE Select ENSP00000271332.3:p.Leu1668=
ENST00000271332.3:c.5002C= ENSP00000271332.3:p.Leu1668=
NM_001408.2:c.5002C= NP_001399.1:p.Leu1668=
XM_005270580.3:c.5002C= XP_005270637.1:p.Leu1668=
NM_001408.3:c.5002C= MANE Select NP_001399.1:p.Leu1668=
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