Canonical Allele Identifier: CA341502148
Gene: CELSR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109264553T>A , CM000663.2:g.109264553T>A GRCh38
NC_000001.10:g.109807175T>A , CM000663.1:g.109807175T>A GRCh37
NC_000001.9:g.109608698T>A NCBI36
NG_052669.1:g.19849T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000271332.4:c.5389T>A MANE Select ENSP00000271332.3:p.Cys1797Ser
ENST00000271332.3:c.5389T>A ENSP00000271332.3:p.Cys1797Ser
NM_001408.2:c.5389T>A NP_001399.1:p.Cys1797Ser
XM_005270580.3:c.5389T>A XP_005270637.1:p.Cys1797Ser
NM_001408.3:c.5389T>A MANE Select NP_001399.1:p.Cys1797Ser