Canonical Allele Identifier: CA10626139

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44144377del , CM000669.2:g.44144377del	GRCh38
NC_000007.13:g.44183976del , CM000669.1:g.44183976del	GRCh37
NC_000007.12:g.44150501del	NCBI36
NG_008847.1:g.50047del
NG_008847.2:g.58794del

Transcript Alleles

HGVS	Amino-acid Change
NM_000162.5:c.*759del MANE Select	NP_000153.1:n.*759del
ENST00000403799.8:c.*759del MANE Select	ENSP00000384247.3:n.*759del
NM_000162.3:c.*759del	NP_000153.1:n.*759del
NM_000162.4:c.*759del	NP_000153.1:n.*759del
NM_001354800.1:c.1370-141del	NP_001341729.1:n.1370-141del
NM_001354801.1:c.*759del	NP_001341730.1:n.*759del
NM_001354802.1:c.230-141del	NP_001341731.1:n.230-141del
NM_001354803.1:c.*759del	NP_001341732.1:n.*759del
NM_001354803.2:c.*759del	NP_001341732.1:n.*759del
NM_033507.1:c.*759del	NP_277042.1:n.*759del
NM_033507.2:c.*759del	NP_277042.1:n.*759del
NM_033507.3:c.*759del	NP_277042.1:n.*759del
NM_033508.1:c.*759del	NP_277043.1:n.*759del
NM_033508.2:c.*759del	NP_277043.1:n.*759del
NM_033508.3:c.*759del	NP_277043.1:n.*759del
ENST00000336642.8:c.1209del	ENSP00000338009.4:n.1209del
ENST00000336642.9:c.*759del	ENSP00000338009.5:n.*759del
ENST00000345378.6:c.*759del	ENSP00000223366.2:n.*759del
ENST00000345378.7:c.*759del	ENSP00000223366.2:n.*759del
ENST00000395796.7:c.*759del	ENSP00000379142.3:n.*759del
ENST00000395796.8:c.*2155del	ENSP00000379142.4:n.*2155del
ENST00000403799.7:c.*759del	ENSP00000384247.3:n.*759del
ENST00000459642.1:n.1537del
ENST00000616242.4:c.2154del	ENSP00000482149.1:n.2154del
ENST00000616242.5:c.*1277del	ENSP00000482149.2:n.*1277del
ENST00000671824.1:c.*759del	ENSP00000500264.1:n.*759del
ENST00000672743.1:n.382-141del
ENST00000673284.1:c.1370-141del	ENSP00000499852.1:n.1370-141del
ENST00000683378.1:n.1383del
XM_024446707.1:c.*759del	XP_024302475.1:n.*759del