Canonical Allele Identifier: CA1323928839

Gene: CRYGD

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.208124085_208124086delinsTG , CM000664.2:g.208124085_208124086delinsTG	GRCh38
NC_000002.11:g.208988809_208988810delinsTG , CM000664.1:g.208988809_208988810delinsTG	GRCh37
NC_000002.10:g.208697054_208697055delinsTG	NCBI36
NG_008039.1:g.5504_5505delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264376.5:c.252+26_252+27delinsCA MANE Select	ENSP00000264376.4:n.252+26_252+27delinsCA
ENST00000264376.4:c.252+26_252+27delinsCA	ENSP00000264376.4:n.252+26_252+27delinsCA
NM_006891.3:c.252+26_252+27delinsCA	NP_008822.2:n.252+26_252+27delinsCA
NR_038437.1:n.97+4860_97+4861delinsTG
NM_006891.4:c.252+26_252+27delinsCA MANE Select	NP_008822.2:n.252+26_252+27delinsCA