Canonical Allele Identifier: CA1426983553
Gene: CRYGS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186539542T= , CM000665.2:g.186539542T= GRCh38
NC_000003.11:g.186257331T= , CM000665.1:g.186257331T= GRCh37
NC_000003.10:g.187740025T= NCBI36
NG_009829.1:g.9837A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307944.6:c.77A= MANE Select ENSP00000312099.5:p.Asp26=
ENST00000307944.5:c.77A= ENSP00000312099.5:p.Asp26=
ENST00000392499.6:c.77A= ENSP00000376287.2:p.Asp26=
ENST00000460288.1:n.979A=
NM_017541.2:c.77A= NP_060011.1:p.Asp26=
NM_017541.3:c.77A= NP_060011.1:p.Asp26=
NM_017541.4:c.77A= MANE Select NP_060011.1:p.Asp26=