Canonical Allele Identifier: CA2817997023
Gene: CRYAA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.43169083T>G , CM000683.2:g.43169083T>G GRCh38
NG_009823.1:g.5053T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000291554.6:c.-17T>G MANE Select ENSP00000291554.2:n.-17T>G
NM_000394.3:c.-17T>G NP_000385.1:n.-17T>G
XR_001755073.1:n.647+1954A>C
NM_000394.4:c.-17T>G MANE Select NP_000385.1:n.-17T>G