Canonical Allele Identifier: CA1022638158
Gene: CRYAA HGNC NCBI

Linked Data

gnomAD v3: 21-43169364-A-C
gnomAD v4: 21-43169364-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.43169364A>C , CM000683.2:g.43169364A>C GRCh38
NG_009823.1:g.5334A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000291554.6:c.189+76A>C MANE Select ENSP00000291554.2:n.189+76A>C
ENST00000482775.1:n.202+76A>C
NM_000394.3:c.189+76A>C NP_000385.1:n.189+76A>C
XR_001755073.1:n.647+1673T>G
NM_000394.4:c.189+76A>C MANE Select NP_000385.1:n.189+76A>C
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