Canonical Allele Identifier: CA2391130649
Gene: CRYAA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.43169019G= , CM000683.2:g.43169019G= GRCh38
NG_009823.1:g.4989G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000291554.6:c.-81G= MANE Select ENSP00000291554.2:n.-81G=
NM_000394.3:c.-81G= NP_000385.1:n.-81G=
XR_001755073.1:n.647+2018C=
NM_000394.4:c.-81G= MANE Select NP_000385.1:n.-81G=