Canonical Allele Identifier: CA1426983543
Gene: CRYGS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186539517T= , CM000665.2:g.186539517T= GRCh38
NC_000003.11:g.186257306T= , CM000665.1:g.186257306T= GRCh37
NC_000003.10:g.187740000T= NCBI36
NG_009829.1:g.9862A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307944.6:c.102A= MANE Select ENSP00000312099.5:p.Leu34=
ENST00000307944.5:c.102A= ENSP00000312099.5:p.Leu34=
ENST00000392499.6:c.102A= ENSP00000376287.2:p.Leu34=
ENST00000460288.1:n.1004A=
NM_017541.2:c.102A= NP_060011.1:p.Leu34=
NM_017541.3:c.102A= NP_060011.1:p.Leu34=
NM_017541.4:c.102A= MANE Select NP_060011.1:p.Leu34=