Canonical Allele Identifier: CA2577985885
Gene: CRYGS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186539579dup , CM000665.2:g.186539579dup GRCh38
NC_000003.11:g.186257368dup , CM000665.1:g.186257368dup GRCh37
NC_000003.10:g.187740062dup NCBI36
NG_009829.1:g.9804dup

Transcript Alleles

HGVS Amino-acid change
ENST00000307944.6:c.44dup MANE Select ENSP00000312099.5:p.Asn15LysfsTer8
ENST00000307944.5:c.44dup ENSP00000312099.5:p.Asn15LysfsTer8
ENST00000392499.6:c.44dup ENSP00000376287.2:p.Asn15LysfsTer8
ENST00000460288.1:n.946dup
NM_017541.2:c.44dup NP_060011.1:p.Asn15LysfsTer8
NM_017541.3:c.44dup NP_060011.1:p.Asn15LysfsTer8
NM_017541.4:c.44dup MANE Select NP_060011.1:p.Asn15LysfsTer8
Search 100 bp 5'
Search 100 bp 3'