Canonical Allele Identifier: CA2662867524
Gene: CRYGD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208124039del , CM000664.2:g.208124039del GRCh38
NC_000002.11:g.208988763del , CM000664.1:g.208988763del GRCh37
NC_000002.10:g.208697008del NCBI36
NG_008039.1:g.5552del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264376.5:c.252+74del MANE Select ENSP00000264376.4:n.252+74del
ENST00000264376.4:c.252+74del ENSP00000264376.4:n.252+74del
NM_006891.3:c.252+74del NP_008822.2:n.252+74del
NR_038437.1:n.97+4814del
NM_006891.4:c.252+74del MANE Select NP_008822.2:n.252+74del