Canonical Allele Identifier: CA2754048844
Gene: CRYGC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208129711_208129713dup , CM000664.2:g.208129711_208129713dup GRCh38
NC_000002.11:g.208994435_208994437dup , CM000664.1:g.208994435_208994437dup GRCh37
NC_000002.10:g.208702680_208702682dup NCBI36
NG_008038.1:g.5118_5120dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000282141.4:c.10-30_10-28dup MANE Select ENSP00000282141.3:n.10-30_10-28dup
ENST00000282141.3:c.10-30_10-28dup ENSP00000282141.3:n.10-30_10-28dup
NM_020989.3:c.10-30_10-28dup NP_066269.1:n.10-30_10-28dup
NR_038437.1:n.98-7345_98-7343dup
XM_011510661.1:c.10-30_10-28dup XP_011508963.1:n.10-30_10-28dup
XM_011510662.1:c.10-30_10-28dup XP_011508964.1:n.10-30_10-28dup
XM_011510663.1:c.-120-30_-120-28dup XP_011508965.1:n.-120-30_-120-28dup
NM_020989.4:c.10-30_10-28dup MANE Select NP_066269.1:n.10-30_10-28dup