Canonical Allele Identifier: CA2391130651
Gene: CRYAA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.43169028T= , CM000683.2:g.43169028T= GRCh38
NG_009823.1:g.4998T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000291554.6:c.-72T= MANE Select ENSP00000291554.2:n.-72T=
NM_000394.3:c.-72T= NP_000385.1:n.-72T=
XR_001755073.1:n.647+2009A=
NM_000394.4:c.-72T= MANE Select NP_000385.1:n.-72T=