Canonical Allele Identifier: CA1426983519
Gene: CRYGS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186539465T= , CM000665.2:g.186539465T= GRCh38
NC_000003.11:g.186257254T= , CM000665.1:g.186257254T= GRCh37
NC_000003.10:g.187739948T= NCBI36
NG_009829.1:g.9914A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307944.6:c.154A= MANE Select ENSP00000312099.5:p.Arg52=
ENST00000307944.5:c.154A= ENSP00000312099.5:p.Arg52=
ENST00000392499.6:c.154A= ENSP00000376287.2:p.Arg52=
ENST00000460288.1:n.1056A=
NM_017541.2:c.154A= NP_060011.1:p.Arg52=
NM_017541.3:c.154A= NP_060011.1:p.Arg52=
NM_017541.4:c.154A= MANE Select NP_060011.1:p.Arg52=