Canonical Allele Identifier: CA1323928905

Gene: CRYGD

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.208124200T= , CM000664.2:g.208124200T=	GRCh38
NC_000002.11:g.208988924T= , CM000664.1:g.208988924T=	GRCh37
NC_000002.10:g.208697169T=	NCBI36
NG_008039.1:g.5390A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264376.5:c.164A= MANE Select	ENSP00000264376.4:p.Gln55=
ENST00000264376.4:c.164A=	ENSP00000264376.4:p.Gln55=
NM_006891.3:c.164A=	NP_008822.2:p.Gln55=
NR_038437.1:n.97+4975T=
NM_006891.4:c.164A= MANE Select	NP_008822.2:p.Gln55=