Canonical Allele Identifier: CA1323928820

Gene: CRYGD

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.208124047_208124049delinsCTT , CM000664.2:g.208124047_208124049delinsCTT	GRCh38
NC_000002.11:g.208988771_208988773delinsCTT , CM000664.1:g.208988771_208988773delinsCTT	GRCh37
NC_000002.10:g.208697016_208697018delinsCTT	NCBI36
NG_008039.1:g.5541_5543delinsAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264376.5:c.252+63_252+65delinsAAG MANE Select	ENSP00000264376.4:n.252+63_252+65delinsAAG
ENST00000264376.4:c.252+63_252+65delinsAAG	ENSP00000264376.4:n.252+63_252+65delinsAAG
NM_006891.3:c.252+63_252+65delinsAAG	NP_008822.2:n.252+63_252+65delinsAAG
NR_038437.1:n.97+4822_97+4824delinsCTT
NM_006891.4:c.252+63_252+65delinsAAG MANE Select	NP_008822.2:n.252+63_252+65delinsAAG