Canonical Allele Identifier: CA1323928801

Gene: CRYGD

Linked Data

• dbSNP Id: rs1694923770

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.208124015_208124016insTA , CM000664.2:g.208124015_208124016insTA	GRCh38
NC_000002.11:g.208988739_208988740insTA , CM000664.1:g.208988739_208988740insTA	GRCh37
NC_000002.10:g.208696984_208696985insTA	NCBI36
NG_008039.1:g.5574_5575insTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264376.5:c.252+96_252+97insTA MANE Select	ENSP00000264376.4:n.252+96_252+97insTA
ENST00000264376.4:c.252+96_252+97insTA	ENSP00000264376.4:n.252+96_252+97insTA
NM_006891.3:c.252+96_252+97insTA	NP_008822.2:n.252+96_252+97insTA
NR_038437.1:n.97+4790_97+4791insTA
NM_006891.4:c.252+96_252+97insTA MANE Select	NP_008822.2:n.252+96_252+97insTA