Canonical Allele Identifier: CA2817997025
Gene: CRYAA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.43169084G>C , CM000683.2:g.43169084G>C GRCh38
NG_009823.1:g.5054G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000291554.6:c.-16G>C MANE Select ENSP00000291554.2:n.-16G>C
NM_000394.3:c.-16G>C NP_000385.1:n.-16G>C
XR_001755073.1:n.647+1953C>G
NM_000394.4:c.-16G>C MANE Select NP_000385.1:n.-16G>C