Canonical Allele Identifier: CA1323931525

Gene: CRYGC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.208129746_208129748delinsACT , CM000664.2:g.208129746_208129748delinsACT	GRCh38
NC_000002.11:g.208994470_208994472delinsACT , CM000664.1:g.208994470_208994472delinsACT	GRCh37
NC_000002.10:g.208702715_208702717delinsACT	NCBI36
NG_008038.1:g.5083_5085delinsAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282141.4:c.9+36_9+38delinsAGT MANE Select	ENSP00000282141.3:n.9+36_9+38delinsAGT
ENST00000282141.3:c.9+36_9+38delinsAGT	ENSP00000282141.3:n.9+36_9+38delinsAGT
NM_020989.3:c.9+36_9+38delinsAGT	NP_066269.1:n.9+36_9+38delinsAGT
NR_038437.1:n.98-7310_98-7308delinsACT
XM_011510661.1:c.9+36_9+38delinsAGT	XP_011508963.1:n.9+36_9+38delinsAGT
XM_011510662.1:c.9+36_9+38delinsAGT	XP_011508964.1:n.9+36_9+38delinsAGT
XM_011510663.1:c.-120-65_-120-63delinsAGT	XP_011508965.1:n.-120-65_-120-63delinsAGT
NM_020989.4:c.9+36_9+38delinsAGT MANE Select	NP_066269.1:n.9+36_9+38delinsAGT