Canonical Allele Identifier: CA2000479041
Gene: CRYAB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.111908744T= , CM000673.2:g.111908744T= GRCh38
NC_000011.9:g.111779468T= , CM000673.1:g.111779468T= GRCh37
NC_000011.8:g.111284678T= NCBI36
NG_009824.2:g.19979A=
NG_033080.1:g.1009T=
NG_009824.3:g.19979A=
NG_033080.2:g.1009T=

Transcript Alleles

HGVS Amino-acid change
ENST00000526167.5:c.*27A= ENSP00000434793.1:n.*27A=
ENST00000526180.6:c.*20A= ENSP00000436051.1:n.*20A=
ENST00000527899.6:c.*20A= ENSP00000436089.2:n.*20A=
ENST00000528961.6:c.*20A= ENSP00000435960.1:n.*20A=
ENST00000533280.6:c.*20A= ENSP00000435046.1:n.*20A=
ENST00000533475.6:c.*20A= ENSP00000433560.1:n.*20A=
ENST00000533879.2:c.*20A= ENSP00000435931.2:n.*20A=
ENST00000533971.2:c.*1439A= ENSP00000434269.1:n.*1439A=
ENST00000616970.5:c.*20A= ENSP00000483554.1:n.*20A=
ENST00000650687.2:c.*20A= MANE Select ENSP00000499082.1:n.*20A=
ENST00000651164.1:c.*20A= ENSP00000498735.1:n.*20A=
ENST00000651650.1:c.*20A= ENSP00000498749.1:n.*20A=
ENST00000652223.1:n.3293A=
ENST00000652606.1:n.1866A=
ENST00000227251.7:c.*20A= ENSP00000227251.3:n.*20A=
ENST00000524660.1:c.339A=
ENST00000525823.1:c.*20A= ENSP00000435411.1:n.*20A=
ENST00000526180.5:c.*20A= ENSP00000436051.1:n.*20A=
ENST00000527950.5:c.*20A= ENSP00000437149.1:n.*20A=
ENST00000531198.5:c.*20A= ENSP00000434247.1:n.*20A=
ENST00000533280.5:c.*20A= ENSP00000435046.1:n.*20A=
ENST00000533475.5:c.*20A= ENSP00000433560.1:n.*20A=
ENST00000616970.4:c.*20A= ENSP00000483554.1:n.*20A=
NM_001289807.1:c.*20A= NP_001276736.1:n.*20A=
NM_001289808.1:c.*20A= NP_001276737.1:n.*20A=
NM_001885.2:c.*20A= NP_001876.1:n.*20A=
XM_011542608.1:c.*20A= XP_011540910.1:n.*20A=
XM_011542609.1:c.*20A= XP_011540911.1:n.*20A=
NM_001330379.1:c.*20A= NP_001317308.1:n.*20A=
NM_001289808.2:c.*20A= MANE Select NP_001276737.1:n.*20A=
NM_001368245.1:c.*20A= NP_001355174.1:n.*20A=
NM_001368246.1:c.*20A= NP_001355175.1:n.*20A=
NM_001885.3:c.*20A= NP_001876.1:n.*20A=