Canonical Allele Identifier: CA2695203135

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44149828_44149832del , CM000669.2:g.44149828_44149832del	GRCh38
NC_000007.13:g.44189427_44189431del , CM000669.1:g.44189427_44189431del	GRCh37
NC_000007.12:g.44155952_44155956del	NCBI36
NG_008847.1:g.44592_44596del
NG_008847.2:g.53339_53343del

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*605_*609del	ENSP00000379142.4:n.*605_*609del
ENST00000616242.5:c.607_611del	ENSP00000482149.2:p.Val203Ter
ENST00000682635.1:n.1093_1097del
ENST00000345378.7:c.610_614del	ENSP00000223366.2:p.Val204Ter
ENST00000403799.8:c.607_611del MANE Select	ENSP00000384247.3:p.Val203Ter
ENST00000671824.1:c.607_611del	ENSP00000500264.1:p.Val203Ter
ENST00000673284.1:c.607_611del	ENSP00000499852.1:p.Val203Ter
ENST00000345378.6:c.610_614del	ENSP00000223366.2:p.Val204Ter
ENST00000395796.7:c.604_608del	ENSP00000379142.3:p.Val202Ter
ENST00000403799.7:c.607_611del	ENSP00000384247.3:p.Val203Ter
ENST00000437084.1:c.556_560del	ENSP00000402840.1:p.Val186Ter
ENST00000616242.4:c.604_608del	ENSP00000482149.1:p.Val202Ter
NM_000162.3:c.607_611del	NP_000153.1:p.Val203Ter
NM_033507.1:c.610_614del	NP_277042.1:p.Val204Ter
NM_033508.1:c.604_608del	NP_277043.1:p.Val202Ter
NM_000162.4:c.607_611del	NP_000153.1:p.Val203Ter
NM_001354800.1:c.607_611del	NP_001341729.1:p.Val203Ter
NM_033507.2:c.610_614del	NP_277042.1:p.Val204Ter
NM_033508.2:c.604_608del	NP_277043.1:p.Val202Ter
NM_000162.5:c.607_611del MANE Select	NP_000153.1:p.Val203Ter
NM_033507.3:c.610_614del	NP_277042.1:p.Val204Ter
NM_033508.3:c.604_608del	NP_277043.1:p.Val202Ter