Canonical Allele Identifier: CA1426983558
Gene: CRYGS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186539548_186539550delinsTCA , CM000665.2:g.186539548_186539550delinsTCA GRCh38
NC_000003.11:g.186257337_186257339delinsTCA , CM000665.1:g.186257337_186257339delinsTCA GRCh37
NC_000003.10:g.187740031_187740033delinsTCA NCBI36
NG_009829.1:g.9829_9831delinsTGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000307944.6:c.69_71delinsTGA MANE Select ENSP00000312099.5:p.Cys23=
ENST00000307944.5:c.69_71delinsTGA ENSP00000312099.5:p.Cys23=
ENST00000392499.6:c.69_71delinsTGA ENSP00000376287.2:p.Cys23=
ENST00000460288.1:n.971_973delinsTGA
NM_017541.2:c.69_71delinsTGA NP_060011.1:p.Cys23=
NM_017541.3:c.69_71delinsTGA NP_060011.1:p.Cys23=
NM_017541.4:c.69_71delinsTGA MANE Select NP_060011.1:p.Cys23=
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