Canonical Allele Identifier: CA2654731608
Gene: CRYAA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.43169491_43169492insTT , CM000683.2:g.43169491_43169492insTT GRCh38
NG_009823.1:g.5461_5462insTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000291554.6:c.189+203_189+204insTT MANE Select ENSP00000291554.2:n.189+203_189+204insTT
ENST00000482775.1:n.203-42_203-41insTT
NM_000394.3:c.189+203_189+204insTT NP_000385.1:n.189+203_189+204insTT
XR_001755073.1:n.647+1545_647+1546insAA
NM_000394.4:c.189+203_189+204insTT MANE Select NP_000385.1:n.189+203_189+204insTT