Canonical Allele Identifier: CA2391130664
Gene: CRYAA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.43169053C= , CM000683.2:g.43169053C= GRCh38
NG_009823.1:g.5023C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000291554.6:c.-47C= MANE Select ENSP00000291554.2:n.-47C=
NM_000394.3:c.-47C= NP_000385.1:n.-47C=
XR_001755073.1:n.647+1984G=
NM_000394.4:c.-47C= MANE Select NP_000385.1:n.-47C=