Canonical Allele Identifier: CA2701438391
Gene: CRYGD HGNC NCBI

Linked Data

dbSNP Id: rs2105853712
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208124125del , CM000664.2:g.208124125del GRCh38
NC_000002.11:g.208988849del , CM000664.1:g.208988849del GRCh37
NC_000002.10:g.208697094del NCBI36
NG_008039.1:g.5465del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264376.5:c.239del MANE Select ENSP00000264376.4:p.Arg80ProfsTer23
ENST00000264376.4:c.239del ENSP00000264376.4:p.Arg80ProfsTer23
NM_006891.3:c.239del NP_008822.2:p.Arg80ProfsTer23
NR_038437.1:n.97+4900del
NM_006891.4:c.239del MANE Select NP_008822.2:p.Arg80ProfsTer23
Search 100 bp 5'
Search 100 bp 3'