Canonical Allele Identifier: CA2662869238
Gene: CRYGC HGNC NCBI

Linked Data

gnomAD v4: 2-208129487-CATT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208129488_208129490del , CM000664.2:g.208129488_208129490del GRCh38
NC_000002.11:g.208994212_208994214del , CM000664.1:g.208994212_208994214del GRCh37
NC_000002.10:g.208702457_208702459del NCBI36
NG_008038.1:g.5341_5343del
NG_008039.1:g.100_102del

Transcript Alleles

HGVS Amino-acid Change
ENST00000282141.4:c.203_205del MANE Select ENSP00000282141.3:p.Gln68_Trp69delinsArg
ENST00000282141.3:c.203_205del ENSP00000282141.3:p.Gln68_Trp69delinsArg
NM_020989.3:c.203_205del NP_066269.1:p.Gln68_Trp69delinsArg
NR_038437.1:n.98-7568_98-7566del
XM_011510661.1:c.203_205del XP_011508963.1:p.Gln68_Trp69delinsArg
XM_011510662.1:c.203_205del XP_011508964.1:p.Gln68_Trp69delinsArg
XM_011510663.1:c.74_76del XP_011508965.1:p.Gln25_Trp26delinsArg
NM_020989.4:c.203_205del MANE Select NP_066269.1:p.Gln68_Trp69delinsArg
Search 100 bp 5'
Search 100 bp 3'