Canonical Allele Identifier: CA1323928857
Gene: CRYGD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208124113_208124115delinsTGG , CM000664.2:g.208124113_208124115delinsTGG GRCh38
NC_000002.11:g.208988837_208988839delinsTGG , CM000664.1:g.208988837_208988839delinsTGG GRCh37
NC_000002.10:g.208697082_208697084delinsTGG NCBI36
NG_008039.1:g.5475_5477delinsCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000264376.5:c.249_251delinsCCA MANE Select ENSP00000264376.4:p.Pro83=
ENST00000264376.4:c.249_251delinsCCA ENSP00000264376.4:p.Pro83=
NM_006891.3:c.249_251delinsCCA NP_008822.2:p.Pro83=
NR_038437.1:n.97+4888_97+4890delinsTGG
NM_006891.4:c.249_251delinsCCA MANE Select NP_008822.2:p.Pro83=