Canonical Allele Identifier: CA2391130879
Gene: CRYAA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.43169596T= , CM000683.2:g.43169596T= GRCh38
NG_009823.1:g.5566T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000291554.6:c.189+308T= MANE Select ENSP00000291554.2:n.189+308T=
ENST00000482775.1:n.266T=
NM_000394.3:c.189+308T= NP_000385.1:n.189+308T=
XR_001755073.1:n.647+1441A=
NM_000394.4:c.189+308T= MANE Select NP_000385.1:n.189+308T=