Canonical Allele Identifier: CA382595858

Gene: CRYAB

Linked Data

• dbSNP Id: rs1592506105
• gnomAD v4: 11-111908837-A-G
• MyVariant Identifiers: chr11:g.111779561A>G (hg19) ; chr11:g.111908837A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.111908837A>G , CM000673.2:g.111908837A>G	GRCh38
NC_000011.9:g.111779561A>G , CM000673.1:g.111779561A>G	GRCh37
NC_000011.8:g.111284771A>G	NCBI36
NG_009824.2:g.19886T>C
NG_033080.1:g.1102A>G
NG_009824.3:g.19886T>C
NG_033080.2:g.1102A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000526167.5:c.254T>C	ENSP00000434793.1:p.Val85Ala
ENST00000526180.6:c.455T>C	ENSP00000436051.1:p.Val152Ala
ENST00000527899.6:c.455T>C	ENSP00000436089.2:p.Val152Ala
ENST00000528961.6:c.254T>C	ENSP00000435960.1:p.Val85Ala
ENST00000533280.6:c.254T>C	ENSP00000435046.1:p.Val85Ala
ENST00000533475.6:c.455T>C	ENSP00000433560.1:p.Val152Ala
ENST00000533879.2:c.455T>C	ENSP00000435931.2:p.Val152Ala
ENST00000533971.2:c.*1346T>C	ENSP00000434269.1:n.*1346T>C
ENST00000616970.5:c.455T>C	ENSP00000483554.1:p.Val152Ala
ENST00000650687.2:c.455T>C MANE Select	ENSP00000499082.1:p.Val152Ala
ENST00000651164.1:c.455T>C	ENSP00000498735.1:p.Val152Ala
ENST00000651650.1:c.254T>C	ENSP00000498749.1:p.Val85Ala
ENST00000652223.1:n.3200T>C
ENST00000652606.1:n.1773T>C
ENST00000227251.7:c.455T>C	ENSP00000227251.3:p.Val152Ala
ENST00000524660.1:c.246T>C
ENST00000525823.1:c.254T>C	ENSP00000435411.1:p.Val85Ala
ENST00000526167.4:c.254T>C	ENSP00000434793.1:p.Val85Ala
ENST00000526180.5:c.455T>C	ENSP00000436051.1:p.Val152Ala
ENST00000527899.5:c.455T>C	ENSP00000436089.1:p.Val152Ala
ENST00000527950.5:c.455T>C	ENSP00000437149.1:p.Val152Ala
ENST00000528961.5:c.254T>C	ENSP00000435960.1:p.Val85Ala
ENST00000531198.5:c.455T>C	ENSP00000434247.1:p.Val152Ala
ENST00000533280.5:c.254T>C	ENSP00000435046.1:p.Val85Ala
ENST00000533475.5:c.455T>C	ENSP00000433560.1:p.Val152Ala
ENST00000616970.4:c.455T>C	ENSP00000483554.1:p.Val152Ala
NM_001289807.1:c.455T>C	NP_001276736.1:p.Val152Ala
NM_001289808.1:c.455T>C	NP_001276737.1:p.Val152Ala
NM_001885.2:c.455T>C	NP_001876.1:p.Val152Ala
XM_011542608.1:c.455T>C	XP_011540910.1:p.Val152Ala
XM_011542609.1:c.254T>C	XP_011540911.1:p.Val85Ala
NM_001330379.1:c.254T>C	NP_001317308.1:p.Val85Ala
NM_001289808.2:c.455T>C MANE Select	NP_001276737.1:p.Val152Ala
NM_001368245.1:c.455T>C	NP_001355174.1:p.Val152Ala
NM_001368246.1:c.254T>C	NP_001355175.1:p.Val85Ala
NM_001885.3:c.455T>C	NP_001876.1:p.Val152Ala