Canonical Allele Identifier: CA1426983555
Gene: CRYGS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186539544G= , CM000665.2:g.186539544G= GRCh38
NC_000003.11:g.186257333G= , CM000665.1:g.186257333G= GRCh37
NC_000003.10:g.187740027G= NCBI36
NG_009829.1:g.9835C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307944.6:c.75C= MANE Select ENSP00000312099.5:p.Cys25=
ENST00000307944.5:c.75C= ENSP00000312099.5:p.Cys25=
ENST00000392499.6:c.75C= ENSP00000376287.2:p.Cys25=
ENST00000460288.1:n.977C=
NM_017541.2:c.75C= NP_060011.1:p.Cys25=
NM_017541.3:c.75C= NP_060011.1:p.Cys25=
NM_017541.4:c.75C= MANE Select NP_060011.1:p.Cys25=