Canonical Allele Identifier: CA645372108
Gene: CRYGC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208129500del , CM000664.2:g.208129500del GRCh38
NC_000002.11:g.208994224del , CM000664.1:g.208994224del GRCh37
NC_000002.10:g.208702469del NCBI36
NG_008038.1:g.5331del
NG_008039.1:g.90del

Transcript Alleles

HGVS Amino-acid Change
ENST00000282141.4:c.193del MANE Select ENSP00000282141.3:p.Asp65ThrfsTer?
ENST00000282141.3:c.193del ENSP00000282141.3:p.Asp65ThrfsTer?
NM_020989.3:c.193del NP_066269.1:p.Asp65ThrfsTer?
NR_038437.1:n.98-7556del
XM_011510661.1:c.193del XP_011508963.1:p.Asp65ThrfsTer?
XM_011510662.1:c.193del XP_011508964.1:p.Asp65ThrfsTer?
XM_011510663.1:c.64del XP_011508965.1:p.Asp22ThrfsTer?
NM_020989.4:c.193del MANE Select NP_066269.1:p.Asp65ThrfsTer?