Canonical Allele Identifier: CA1323931527

Gene: CRYGC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.208129747_208129748delinsCT , CM000664.2:g.208129747_208129748delinsCT	GRCh38
NC_000002.11:g.208994471_208994472delinsCT , CM000664.1:g.208994471_208994472delinsCT	GRCh37
NC_000002.10:g.208702716_208702717delinsCT	NCBI36
NG_008038.1:g.5083_5084delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282141.4:c.9+36_9+37delinsAG MANE Select	ENSP00000282141.3:n.9+36_9+37delinsAG
ENST00000282141.3:c.9+36_9+37delinsAG	ENSP00000282141.3:n.9+36_9+37delinsAG
NM_020989.3:c.9+36_9+37delinsAG	NP_066269.1:n.9+36_9+37delinsAG
NR_038437.1:n.98-7309_98-7308delinsCT
XM_011510661.1:c.9+36_9+37delinsAG	XP_011508963.1:n.9+36_9+37delinsAG
XM_011510662.1:c.9+36_9+37delinsAG	XP_011508964.1:n.9+36_9+37delinsAG
XM_011510663.1:c.-120-65_-120-64delinsAG	XP_011508965.1:n.-120-65_-120-64delinsAG
NM_020989.4:c.9+36_9+37delinsAG MANE Select	NP_066269.1:n.9+36_9+37delinsAG