Canonical Allele Identifier: CA1323931457
Gene: CRYGC HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208129606_208129607delinsAT , CM000664.2:g.208129606_208129607delinsAT GRCh38
NC_000002.11:g.208994330_208994331delinsAT , CM000664.1:g.208994330_208994331delinsAT GRCh37
NC_000002.10:g.208702575_208702576delinsAT NCBI36
NG_008038.1:g.5224_5225delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000282141.4:c.86_87delinsAT MANE Select ENSP00000282141.3:p.Tyr29=
ENST00000282141.3:c.86_87delinsAT ENSP00000282141.3:p.Tyr29=
NM_020989.3:c.86_87delinsAT NP_066269.1:p.Tyr29=
NR_038437.1:n.98-7450_98-7449delinsAT
XM_011510661.1:c.86_87delinsAT XP_011508963.1:p.Tyr29=
XM_011510662.1:c.86_87delinsAT XP_011508964.1:p.Tyr29=
XM_011510663.1:c.-44_-43delinsAT XP_011508965.1:n.-44_-43delinsAT
NM_020989.4:c.86_87delinsAT MANE Select NP_066269.1:p.Tyr29=
Search 100 bp 5'
Search 100 bp 3'