Canonical Allele Identifier: CA2654731431
Gene: CRYAA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.43169066C>A , CM000683.2:g.43169066C>A GRCh38
NG_009823.1:g.5036C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000291554.6:c.-34C>A MANE Select ENSP00000291554.2:n.-34C>A
NM_000394.3:c.-34C>A NP_000385.1:n.-34C>A
XR_001755073.1:n.647+1971G>T
NM_000394.4:c.-34C>A MANE Select NP_000385.1:n.-34C>A