Canonical Allele Identifier: CA1426983542
Gene: CRYGS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186539515_186539517delinsCTT , CM000665.2:g.186539515_186539517delinsCTT GRCh38
NC_000003.11:g.186257304_186257306delinsCTT , CM000665.1:g.186257304_186257306delinsCTT GRCh37
NC_000003.10:g.187739998_187740000delinsCTT NCBI36
NG_009829.1:g.9862_9864delinsAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000307944.6:c.102_104delinsAAG MANE Select ENSP00000312099.5:p.Leu34=
ENST00000307944.5:c.102_104delinsAAG ENSP00000312099.5:p.Leu34=
ENST00000392499.6:c.102_104delinsAAG ENSP00000376287.2:p.Leu34=
ENST00000460288.1:n.1004_1006delinsAAG
NM_017541.2:c.102_104delinsAAG NP_060011.1:p.Leu34=
NM_017541.3:c.102_104delinsAAG NP_060011.1:p.Leu34=
NM_017541.4:c.102_104delinsAAG MANE Select NP_060011.1:p.Leu34=
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