Canonical Allele Identifier: CA1426983521
Gene: CRYGS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186539474_186539475delinsCA , CM000665.2:g.186539474_186539475delinsCA GRCh38
NC_000003.11:g.186257263_186257264delinsCA , CM000665.1:g.186257263_186257264delinsCA GRCh37
NC_000003.10:g.187739957_187739958delinsCA NCBI36
NG_009829.1:g.9904_9905delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000307944.6:c.144_145delinsTG MANE Select ENSP00000312099.5:p.Ala48=
ENST00000307944.5:c.144_145delinsTG ENSP00000312099.5:p.Ala48=
ENST00000392499.6:c.144_145delinsTG ENSP00000376287.2:p.Ala48=
ENST00000460288.1:n.1046_1047delinsTG
NM_017541.2:c.144_145delinsTG NP_060011.1:p.Ala48=
NM_017541.3:c.144_145delinsTG NP_060011.1:p.Ala48=
NM_017541.4:c.144_145delinsTG MANE Select NP_060011.1:p.Ala48=
Search 100 bp 5'
Search 100 bp 3'