Canonical Allele Identifier: CA2391131582
Gene: CRYAA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.43172043C= , CM000683.2:g.43172043C= GRCh38
NG_009823.1:g.8013C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000291554.6:c.313-28C= MANE Select ENSP00000291554.2:n.313-28C=
ENST00000398132.1:c.202-28C= ENSP00000381200.1:n.202-28C=
ENST00000398133.5:c.253-28C= ENSP00000381201.1:n.253-28C=
ENST00000468016.1:n.414-28C=
ENST00000482775.1:n.394-28C=
NM_000394.3:c.313-28C= NP_000385.1:n.313-28C=
XM_005261093.2:c.202-28C= XP_005261150.1:n.202-28C=
NM_001363766.1:c.202-28C= NP_001350695.1:n.202-28C=
NM_000394.4:c.313-28C= MANE Select NP_000385.1:n.313-28C=
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