Canonical Allele Identifier: CA657672468
Gene: CRYAA HGNC NCBI

Linked Data

COSMIC: COSN22987807
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.43169096_43169097insT , CM000683.2:g.43169096_43169097insT GRCh38
NG_009823.1:g.5066_5067insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000291554.6:c.-4_-3insT MANE Select ENSP00000291554.2:n.-4_-3insT
ENST00000482775.1:n.10_11insT
NM_000394.3:c.-4_-3insT NP_000385.1:n.-4_-3insT
XR_001755073.1:n.647+1940_647+1941insA
NM_000394.4:c.-4_-3insT MANE Select NP_000385.1:n.-4_-3insT
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