Canonical Allele Identifier: CA382595347

Gene: CRYAB

Linked Data

• MyVariant Identifiers: chr11:g.111779501G>A (hg19) ; chr11:g.111908777G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.111908777G>A , CM000673.2:g.111908777G>A	GRCh38
NC_000011.9:g.111779501G>A , CM000673.1:g.111779501G>A	GRCh37
NC_000011.8:g.111284711G>A	NCBI36
NG_009824.2:g.19946C>T
NG_033080.1:g.1042G>A
NG_009824.3:g.19946C>T
NG_033080.2:g.1042G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000526167.5:c.314C>T	ENSP00000434793.1:p.Ala105Val
ENST00000526180.6:c.515C>T	ENSP00000436051.1:p.Ala172Val
ENST00000527899.6:c.515C>T	ENSP00000436089.2:p.Ala172Val
ENST00000528961.6:c.314C>T	ENSP00000435960.1:p.Ala105Val
ENST00000533280.6:c.314C>T	ENSP00000435046.1:p.Ala105Val
ENST00000533475.6:c.515C>T	ENSP00000433560.1:p.Ala172Val
ENST00000533879.2:c.515C>T	ENSP00000435931.2:p.Ala172Val
ENST00000533971.2:c.*1406C>T	ENSP00000434269.1:n.*1406C>T
ENST00000616970.5:c.515C>T	ENSP00000483554.1:p.Ala172Val
ENST00000650687.2:c.515C>T MANE Select	ENSP00000499082.1:p.Ala172Val
ENST00000651164.1:c.515C>T	ENSP00000498735.1:p.Ala172Val
ENST00000651650.1:c.314C>T	ENSP00000498749.1:p.Ala105Val
ENST00000652223.1:n.3260C>T
ENST00000652606.1:n.1833C>T
ENST00000227251.7:c.515C>T	ENSP00000227251.3:p.Ala172Val
ENST00000524660.1:c.306C>T
ENST00000525823.1:c.314C>T	ENSP00000435411.1:p.Ala105Val
ENST00000526167.4:c.314C>T	ENSP00000434793.1:p.Ala105Val
ENST00000526180.5:c.515C>T	ENSP00000436051.1:p.Ala172Val
ENST00000527899.5:c.515C>T	ENSP00000436089.1:p.Ala172Val
ENST00000527950.5:c.515C>T	ENSP00000437149.1:p.Ala172Val
ENST00000528961.5:c.314C>T	ENSP00000435960.1:p.Ala105Val
ENST00000531198.5:c.515C>T	ENSP00000434247.1:p.Ala172Val
ENST00000533280.5:c.314C>T	ENSP00000435046.1:p.Ala105Val
ENST00000533475.5:c.515C>T	ENSP00000433560.1:p.Ala172Val
ENST00000616970.4:c.515C>T	ENSP00000483554.1:p.Ala172Val
NM_001289807.1:c.515C>T	NP_001276736.1:p.Ala172Val
NM_001289808.1:c.515C>T	NP_001276737.1:p.Ala172Val
NM_001885.2:c.515C>T	NP_001876.1:p.Ala172Val
XM_011542608.1:c.515C>T	XP_011540910.1:p.Ala172Val
XM_011542609.1:c.314C>T	XP_011540911.1:p.Ala105Val
NM_001330379.1:c.314C>T	NP_001317308.1:p.Ala105Val
NM_001289808.2:c.515C>T MANE Select	NP_001276737.1:p.Ala172Val
NM_001368245.1:c.515C>T	NP_001355174.1:p.Ala172Val
NM_001368246.1:c.314C>T	NP_001355175.1:p.Ala105Val
NM_001885.3:c.515C>T	NP_001876.1:p.Ala172Val