Canonical Allele Identifier: CA6275444

Gene: CRYAB

Linked Data

• dbSNP Id: rs782446124
• ExAC: 11:111779461 T / TA
• gnomAD v2: 11-111779461-T-TA
• gnomAD v3: 11-111908737-T-TA
• gnomAD v4: 11-111908737-T-TA
• MyVariant Identifiers: chr11:g.111779461_111779462insA (hg19) ; chr11:g.111908737_111908738insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.111908743dup , CM000673.2:g.111908743dup	GRCh38
NC_000011.9:g.111779467dup , CM000673.1:g.111779467dup	GRCh37
NC_000011.8:g.111284677dup	NCBI36
NG_009824.2:g.19985dup
NG_033080.1:g.1008dup
NG_009824.3:g.19985dup
NG_033080.2:g.1008dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000526167.5:c.*33dup	ENSP00000434793.1:n.*33dup
ENST00000526180.6:c.*26dup	ENSP00000436051.1:n.*26dup
ENST00000527899.6:c.*26dup	ENSP00000436089.2:n.*26dup
ENST00000528961.6:c.*26dup	ENSP00000435960.1:n.*26dup
ENST00000533280.6:c.*26dup	ENSP00000435046.1:n.*26dup
ENST00000533475.6:c.*26dup	ENSP00000433560.1:n.*26dup
ENST00000533879.2:c.*26dup	ENSP00000435931.2:n.*26dup
ENST00000533971.2:c.*1445dup	ENSP00000434269.1:n.*1445dup
ENST00000616970.5:c.*26dup	ENSP00000483554.1:n.*26dup
ENST00000650687.2:c.*26dup MANE Select	ENSP00000499082.1:n.*26dup
ENST00000651164.1:c.*26dup	ENSP00000498735.1:n.*26dup
ENST00000651650.1:c.*26dup	ENSP00000498749.1:n.*26dup
ENST00000652223.1:n.3299dup
ENST00000652606.1:n.1872dup
ENST00000227251.7:c.*26dup	ENSP00000227251.3:n.*26dup
ENST00000524660.1:c.345dup
ENST00000525823.1:c.*26dup	ENSP00000435411.1:n.*26dup
ENST00000526180.5:c.*26dup	ENSP00000436051.1:n.*26dup
ENST00000527950.5:c.*26dup	ENSP00000437149.1:n.*26dup
ENST00000531198.5:c.*26dup	ENSP00000434247.1:n.*26dup
ENST00000533280.5:c.*26dup	ENSP00000435046.1:n.*26dup
ENST00000533475.5:c.*26dup	ENSP00000433560.1:n.*26dup
ENST00000616970.4:c.*26dup	ENSP00000483554.1:n.*26dup
NM_001289807.1:c.*26dup	NP_001276736.1:n.*26dup
NM_001289808.1:c.*26dup	NP_001276737.1:n.*26dup
NM_001885.2:c.*26dup	NP_001876.1:n.*26dup
XM_011542608.1:c.*26dup	XP_011540910.1:n.*26dup
XM_011542609.1:c.*26dup	XP_011540911.1:n.*26dup
NM_001330379.1:c.*26dup	NP_001317308.1:n.*26dup
NM_001289808.2:c.*26dup MANE Select	NP_001276737.1:n.*26dup
NM_001368245.1:c.*26dup	NP_001355174.1:n.*26dup
NM_001368246.1:c.*26dup	NP_001355175.1:n.*26dup
NM_001885.3:c.*26dup	NP_001876.1:n.*26dup