Canonical Allele Identifier: CA350097693
Gene: CRYGC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208129703_208129706del , CM000664.2:g.208129703_208129706del GRCh38
NC_000002.11:g.208994427_208994430del , CM000664.1:g.208994427_208994430del GRCh37
NC_000002.10:g.208702672_208702675del NCBI36
NG_008038.1:g.5125_5128del

Transcript Alleles

HGVS Amino-acid change
ENST00000282141.4:c.10-23_10-20del MANE Select ENSP00000282141.3:n.10-23_10-20del
ENST00000282141.3:c.10-23_10-20del ENSP00000282141.3:n.10-23_10-20del
NM_020989.3:c.10-23_10-20del NP_066269.1:n.10-23_10-20del
NR_038437.1:n.98-7353_98-7350del
XM_011510661.1:c.10-23_10-20del XP_011508963.1:n.10-23_10-20del
XM_011510662.1:c.10-23_10-20del XP_011508964.1:n.10-23_10-20del
XM_011510663.1:c.-120-23_-120-20del XP_011508965.1:n.-120-23_-120-20del
NM_020989.4:c.10-23_10-20del MANE Select NP_066269.1:n.10-23_10-20del