Canonical Allele Identifier: CA1426983556
Gene: CRYGS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186539545C= , CM000665.2:g.186539545C= GRCh38
NC_000003.11:g.186257334C= , CM000665.1:g.186257334C= GRCh37
NC_000003.10:g.187740028C= NCBI36
NG_009829.1:g.9834G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307944.6:c.74G= MANE Select ENSP00000312099.5:p.Cys25=
ENST00000307944.5:c.74G= ENSP00000312099.5:p.Cys25=
ENST00000392499.6:c.74G= ENSP00000376287.2:p.Cys25=
ENST00000460288.1:n.976G=
NM_017541.2:c.74G= NP_060011.1:p.Cys25=
NM_017541.3:c.74G= NP_060011.1:p.Cys25=
NM_017541.4:c.74G= MANE Select NP_060011.1:p.Cys25=