Canonical Allele Identifier: CA2077975
Gene: CRYGC HGNC NCBI

Linked Data

dbSNP Id: rs761398443

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208129702_208129705del , CM000664.2:g.208129702_208129705del GRCh38
NC_000002.11:g.208994426_208994429del , CM000664.1:g.208994426_208994429del GRCh37
NC_000002.10:g.208702671_208702674del NCBI36
NG_008038.1:g.5126_5129del

Transcript Alleles

HGVS Amino-acid change
ENST00000282141.4:c.10-22_10-19del MANE Select ENSP00000282141.3:n.10-22_10-19del
ENST00000282141.3:c.10-22_10-19del ENSP00000282141.3:n.10-22_10-19del
NM_020989.3:c.10-22_10-19del NP_066269.1:n.10-22_10-19del
NR_038437.1:n.98-7354_98-7351del
XM_011510661.1:c.10-22_10-19del XP_011508963.1:n.10-22_10-19del
XM_011510662.1:c.10-22_10-19del XP_011508964.1:n.10-22_10-19del
XM_011510663.1:c.-120-22_-120-19del XP_011508965.1:n.-120-22_-120-19del
NM_020989.4:c.10-22_10-19del MANE Select NP_066269.1:n.10-22_10-19del