Canonical Allele Identifier: CA2695203062

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44146494_44146511del , CM000669.2:g.44146494_44146511del	GRCh38
NC_000007.13:g.44186093_44186110del , CM000669.1:g.44186093_44186110del	GRCh37
NC_000007.12:g.44152618_44152635del	NCBI36
NG_008847.1:g.47914_47931del
NG_008847.2:g.56661_56678del

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*970_*987del	ENSP00000379142.4:n.*970_*987del
ENST00000616242.5:c.*92_*109del	ENSP00000482149.2:n.*92_*109del
ENST00000683378.1:n.198_215del
ENST00000345378.7:c.975_992del	ENSP00000223366.2:p.Arg326_Phe331del
ENST00000403799.8:c.972_989del MANE Select	ENSP00000384247.3:p.Arg325_Phe330del
ENST00000671824.1:c.1035_1052del	ENSP00000500264.1:p.Arg346_Phe351del
ENST00000673284.1:c.972_989del	ENSP00000499852.1:p.Arg325_Phe330del
ENST00000345378.6:c.975_992del	ENSP00000223366.2:p.Arg326_Phe331del
ENST00000395796.7:c.969_986del	ENSP00000379142.3:p.Arg324_Phe329del
ENST00000403799.7:c.972_989del	ENSP00000384247.3:p.Arg325_Phe330del
ENST00000437084.1:c.921_938del	ENSP00000402840.1:p.Arg308_Phe313del
ENST00000473353.1:n.270_287del
ENST00000616242.4:c.969_986del	ENSP00000482149.1:p.Arg324_Phe329del
NM_000162.3:c.972_989del	NP_000153.1:p.Arg325_Phe330del
NM_033507.1:c.975_992del	NP_277042.1:p.Arg326_Phe331del
NM_033508.1:c.969_986del	NP_277043.1:p.Arg324_Phe329del
NM_000162.4:c.972_989del	NP_000153.1:p.Arg325_Phe330del
NM_001354800.1:c.972_989del	NP_001341729.1:p.Arg325_Phe330del
NM_001354801.1:c.8+109_8+126del	NP_001341730.1:n.8+109_8+126del
NM_033507.2:c.975_992del	NP_277042.1:p.Arg326_Phe331del
NM_033508.2:c.969_986del	NP_277043.1:p.Arg324_Phe329del
NM_000162.5:c.972_989del MANE Select	NP_000153.1:p.Arg325_Phe330del
NM_033507.3:c.975_992del	NP_277042.1:p.Arg326_Phe331del
NM_033508.3:c.969_986del	NP_277043.1:p.Arg324_Phe329del