Canonical Allele Identifier: CA2695203064

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44146547del , CM000669.2:g.44146547del	GRCh38
NC_000007.13:g.44186146del , CM000669.1:g.44186146del	GRCh37
NC_000007.12:g.44152671del	NCBI36
NG_008847.1:g.47880del
NG_008847.2:g.56627del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*936del	ENSP00000379142.4:n.*936del
ENST00000616242.5:c.*58del	ENSP00000482149.2:n.*58del
ENST00000683378.1:n.164del
ENST00000345378.7:c.941del	ENSP00000223366.2:p.Asn314ThrfsTer?
ENST00000403799.8:c.938del MANE Select	ENSP00000384247.3:p.Asn313ThrfsTer?
ENST00000671824.1:c.1001del	ENSP00000500264.1:p.Asn334ThrfsTer?
ENST00000673284.1:c.938del	ENSP00000499852.1:p.Asn313ThrfsTer?
ENST00000345378.6:c.941del	ENSP00000223366.2:p.Asn314ThrfsTer?
ENST00000395796.7:c.935del	ENSP00000379142.3:p.Asn312ThrfsTer?
ENST00000403799.7:c.938del	ENSP00000384247.3:p.Asn313ThrfsTer?
ENST00000437084.1:c.887del	ENSP00000402840.1:p.Asn296ThrfsTer?
ENST00000473353.1:n.236del
ENST00000616242.4:c.935del	ENSP00000482149.1:p.Asn312ThrfsTer?
NM_000162.3:c.938del	NP_000153.1:p.Asn313ThrfsTer?
NM_033507.1:c.941del	NP_277042.1:p.Asn314ThrfsTer?
NM_033508.1:c.935del	NP_277043.1:p.Asn312ThrfsTer?
NM_000162.4:c.938del	NP_000153.1:p.Asn313ThrfsTer?
NM_001354800.1:c.938del	NP_001341729.1:p.Asn313ThrfsTer?
NM_001354801.1:c.8+75del	NP_001341730.1:n.8+75del
NM_033507.2:c.941del	NP_277042.1:p.Asn314ThrfsTer?
NM_033508.2:c.935del	NP_277043.1:p.Asn312ThrfsTer?
NM_000162.5:c.938del MANE Select	NP_000153.1:p.Asn313ThrfsTer?
NM_033507.3:c.941del	NP_277042.1:p.Asn314ThrfsTer?
NM_033508.3:c.935del	NP_277043.1:p.Asn312ThrfsTer?