Canonical Allele Identifier: CA2662867428

Gene: CRYGD

Linked Data

• gnomAD v4: 2-208123997-C-CG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.208123997_208123998insG , CM000664.2:g.208123997_208123998insG	GRCh38
NC_000002.11:g.208988721_208988722insG , CM000664.1:g.208988721_208988722insG	GRCh37
NC_000002.10:g.208696966_208696967insG	NCBI36
NG_008039.1:g.5592_5593insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264376.5:c.252+114_252+115insC MANE Select	ENSP00000264376.4:n.252+114_252+115insC
ENST00000264376.4:c.252+114_252+115insC	ENSP00000264376.4:n.252+114_252+115insC
NM_006891.3:c.252+114_252+115insC	NP_008822.2:n.252+114_252+115insC
NR_038437.1:n.97+4772_97+4773insG
NM_006891.4:c.252+114_252+115insC MANE Select	NP_008822.2:n.252+114_252+115insC