Canonical Allele Identifier: CA1703636117

Gene: GCK

Linked Data

• dbSNP Id: rs2096279182

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44150285_44150287del , CM000669.2:g.44150285_44150287del	GRCh38
NC_000007.13:g.44189884_44189886del , CM000669.1:g.44189884_44189886del	GRCh37
NC_000007.12:g.44156409_44156411del	NCBI36
NG_008847.1:g.44140_44142del
NG_008847.2:g.52887_52889del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*482-220_*482-218del	ENSP00000379142.4:n.*482-220_*482-218del
ENST00000616242.5:c.484-220_484-218del	ENSP00000482149.2:n.484-220_484-218del
ENST00000682635.1:n.970-220_970-218del
ENST00000345378.7:c.487-220_487-218del	ENSP00000223366.2:n.487-220_487-218del
ENST00000403799.8:c.484-220_484-218del MANE Select	ENSP00000384247.3:n.484-220_484-218del
ENST00000671824.1:c.484-220_484-218del	ENSP00000500264.1:n.484-220_484-218del
ENST00000673284.1:c.484-220_484-218del	ENSP00000499852.1:n.484-220_484-218del
ENST00000345378.6:c.487-220_487-218del	ENSP00000223366.2:n.487-220_487-218del
ENST00000395796.7:c.481-220_481-218del	ENSP00000379142.3:n.481-220_481-218del
ENST00000403799.7:c.484-220_484-218del	ENSP00000384247.3:n.484-220_484-218del
ENST00000437084.1:c.433-220_433-218del	ENSP00000402840.1:n.433-220_433-218del
ENST00000616242.4:c.481-220_481-218del	ENSP00000482149.1:n.481-220_481-218del
NM_000162.3:c.484-220_484-218del	NP_000153.1:n.484-220_484-218del
NM_033507.1:c.487-220_487-218del	NP_277042.1:n.487-220_487-218del
NM_033508.1:c.481-220_481-218del	NP_277043.1:n.481-220_481-218del
NM_000162.4:c.484-220_484-218del	NP_000153.1:n.484-220_484-218del
NM_001354800.1:c.484-220_484-218del	NP_001341729.1:n.484-220_484-218del
NM_033507.2:c.487-220_487-218del	NP_277042.1:n.487-220_487-218del
NM_033508.2:c.481-220_481-218del	NP_277043.1:n.481-220_481-218del
NM_000162.5:c.484-220_484-218del MANE Select	NP_000153.1:n.484-220_484-218del
NM_033507.3:c.487-220_487-218del	NP_277042.1:n.487-220_487-218del
NM_033508.3:c.481-220_481-218del	NP_277043.1:n.481-220_481-218del