Canonical Allele Identifier: CA2695203007

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44152361_44152370del , CM000669.2:g.44152361_44152370del	GRCh38
NC_000007.13:g.44191960_44191969del , CM000669.1:g.44191960_44191969del	GRCh37
NC_000007.12:g.44158485_44158494del	NCBI36
NG_008847.1:g.42056_42065del
NG_008847.2:g.50803_50812del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*264_*273del	ENSP00000379142.4:n.*264_*273del
ENST00000616242.5:c.266_275del	ENSP00000482149.2:p.Val89GlufsTer10
ENST00000682635.1:n.752_761del
ENST00000345378.7:c.269_278del	ENSP00000223366.2:p.Val90GlufsTer10
ENST00000403799.8:c.266_275del MANE Select	ENSP00000384247.3:p.Val89GlufsTer10
ENST00000671824.1:c.266_275del	ENSP00000500264.1:p.Val89GlufsTer10
ENST00000673284.1:c.266_275del	ENSP00000499852.1:p.Val89GlufsTer10
ENST00000345378.6:c.269_278del	ENSP00000223366.2:p.Val90GlufsTer10
ENST00000395796.7:c.263_272del	ENSP00000379142.3:p.Val88GlufsTer10
ENST00000403799.7:c.266_275del	ENSP00000384247.3:p.Val89GlufsTer10
ENST00000437084.1:c.266_275del	ENSP00000402840.1:p.Val89GlufsTer10
ENST00000616242.4:c.263_272del	ENSP00000482149.1:p.Val88GlufsTer10
NM_000162.3:c.266_275del	NP_000153.1:p.Val89GlufsTer10
NM_033507.1:c.269_278del	NP_277042.1:p.Val90GlufsTer10
NM_033508.1:c.263_272del	NP_277043.1:p.Val88GlufsTer10
NM_000162.4:c.266_275del	NP_000153.1:p.Val89GlufsTer10
NM_001354800.1:c.266_275del	NP_001341729.1:p.Val89GlufsTer10
NM_033507.2:c.269_278del	NP_277042.1:p.Val90GlufsTer10
NM_033508.2:c.263_272del	NP_277043.1:p.Val88GlufsTer10
NM_000162.5:c.266_275del MANE Select	NP_000153.1:p.Val89GlufsTer10
NM_033507.3:c.269_278del	NP_277042.1:p.Val90GlufsTer10
NM_033508.3:c.263_272del	NP_277043.1:p.Val88GlufsTer10