Canonical Allele Identifier: CA2586971172
Gene: CRYGC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208129514del , CM000664.2:g.208129514del GRCh38
NC_000002.11:g.208994238del , CM000664.1:g.208994238del GRCh37
NC_000002.10:g.208702483del NCBI36
NG_008038.1:g.5317del
NG_008039.1:g.76del

Transcript Alleles

HGVS Amino-acid Change
ENST00000282141.4:c.179del MANE Select ENSP00000282141.3:p.Arg60GlnfsTer?
ENST00000282141.3:c.179del ENSP00000282141.3:p.Arg60GlnfsTer?
NM_020989.3:c.179del NP_066269.1:p.Arg60GlnfsTer?
NR_038437.1:n.98-7542del
XM_011510661.1:c.179del XP_011508963.1:p.Arg60GlnfsTer?
XM_011510662.1:c.179del XP_011508964.1:p.Arg60GlnfsTer?
XM_011510663.1:c.50del XP_011508965.1:p.Arg17GlnfsTer?
NM_020989.4:c.179del MANE Select NP_066269.1:p.Arg60GlnfsTer?