Canonical Allele Identifier: CA2391130759
Gene: CRYAA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.43169302C= , CM000683.2:g.43169302C= GRCh38
NG_009823.1:g.5272C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000291554.6:c.189+14C= MANE Select ENSP00000291554.2:n.189+14C=
ENST00000482775.1:n.202+14C=
NM_000394.3:c.189+14C= NP_000385.1:n.189+14C=
XR_001755073.1:n.647+1735G=
NM_000394.4:c.189+14C= MANE Select NP_000385.1:n.189+14C=