Canonical Allele Identifier: CA1323931502

Gene: CRYGC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.208129701_208129705delinsTTCCG , CM000664.2:g.208129701_208129705delinsTTCCG	GRCh38
NC_000002.11:g.208994425_208994429delinsTTCCG , CM000664.1:g.208994425_208994429delinsTTCCG	GRCh37
NC_000002.10:g.208702670_208702674delinsTTCCG	NCBI36
NG_008038.1:g.5126_5130delinsCGGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282141.4:c.10-22_10-18delinsCGGAA MANE Select	ENSP00000282141.3:n.10-22_10-18delinsCGGAA
ENST00000282141.3:c.10-22_10-18delinsCGGAA	ENSP00000282141.3:n.10-22_10-18delinsCGGAA
NM_020989.3:c.10-22_10-18delinsCGGAA	NP_066269.1:n.10-22_10-18delinsCGGAA
NR_038437.1:n.98-7355_98-7351delinsTTCCG
XM_011510661.1:c.10-22_10-18delinsCGGAA	XP_011508963.1:n.10-22_10-18delinsCGGAA
XM_011510662.1:c.10-22_10-18delinsCGGAA	XP_011508964.1:n.10-22_10-18delinsCGGAA
XM_011510663.1:c.-120-22_-120-18delinsCGGAA	XP_011508965.1:n.-120-22_-120-18delinsCGGAA
NM_020989.4:c.10-22_10-18delinsCGGAA MANE Select	NP_066269.1:n.10-22_10-18delinsCGGAA