Canonical Allele Identifier: CA1323928803

Gene: CRYGD

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.208124019_208124020delinsGT , CM000664.2:g.208124019_208124020delinsGT	GRCh38
NC_000002.11:g.208988743_208988744delinsGT , CM000664.1:g.208988743_208988744delinsGT	GRCh37
NC_000002.10:g.208696988_208696989delinsGT	NCBI36
NG_008039.1:g.5570_5571delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264376.5:c.252+92_252+93delinsAC MANE Select	ENSP00000264376.4:n.252+92_252+93delinsAC
ENST00000264376.4:c.252+92_252+93delinsAC	ENSP00000264376.4:n.252+92_252+93delinsAC
NM_006891.3:c.252+92_252+93delinsAC	NP_008822.2:n.252+92_252+93delinsAC
NR_038437.1:n.97+4794_97+4795delinsGT
NM_006891.4:c.252+92_252+93delinsAC MANE Select	NP_008822.2:n.252+92_252+93delinsAC