Canonical Allele Identifier: CA1323928792

Gene: CRYGD

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.208124010_208124012delinsTCA , CM000664.2:g.208124010_208124012delinsTCA	GRCh38
NC_000002.11:g.208988734_208988736delinsTCA , CM000664.1:g.208988734_208988736delinsTCA	GRCh37
NC_000002.10:g.208696979_208696981delinsTCA	NCBI36
NG_008039.1:g.5578_5580delinsTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264376.5:c.252+100_252+102delinsTGA MANE Select	ENSP00000264376.4:n.252+100_252+102delinsTGA
ENST00000264376.4:c.252+100_252+102delinsTGA	ENSP00000264376.4:n.252+100_252+102delinsTGA
NM_006891.3:c.252+100_252+102delinsTGA	NP_008822.2:n.252+100_252+102delinsTGA
NR_038437.1:n.97+4785_97+4787delinsTCA
NM_006891.4:c.252+100_252+102delinsTGA MANE Select	NP_008822.2:n.252+100_252+102delinsTGA