Canonical Allele Identifier: CA2654731623
Gene: CRYAA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.43169503_43169504insTTTC , CM000683.2:g.43169503_43169504insTTTC GRCh38
NG_009823.1:g.5473_5474insTTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000291554.6:c.189+215_189+216insTTTC MANE Select ENSP00000291554.2:n.189+215_189+216insTTTC
ENST00000482775.1:n.203-30_203-29insTTTC
NM_000394.3:c.189+215_189+216insTTTC NP_000385.1:n.189+215_189+216insTTTC
XR_001755073.1:n.647+1534_647+1535insAAAG
NM_000394.4:c.189+215_189+216insTTTC MANE Select NP_000385.1:n.189+215_189+216insTTTC