Canonical Allele Identifier: CA2391131813
Gene: CRYAA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.43172803C= , CM000683.2:g.43172803C= GRCh38
NG_009823.1:g.8773C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000291554.6:c.*523C= MANE Select ENSP00000291554.2:n.*523C=
ENST00000482775.1:n.1126C=
NM_000394.3:c.*523C= NP_000385.1:n.*523C=
XM_005261093.2:c.*523C= XP_005261150.1:n.*523C=
NM_001363766.1:c.*523C= NP_001350695.1:n.*523C=
NM_000394.4:c.*523C= MANE Select NP_000385.1:n.*523C=
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