Canonical Allele Identifier: CA2695202964

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145251_44145259dup , CM000669.2:g.44145251_44145259dup	GRCh38
NC_000007.13:g.44184850_44184858dup , CM000669.1:g.44184850_44184858dup	GRCh37
NC_000007.12:g.44151375_44151383dup	NCBI36
NG_008847.1:g.49168_49176dup
NG_008847.2:g.57915_57923dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1276_*1284dup	ENSP00000379142.4:n.*1276_*1284dup
ENST00000616242.5:c.*398_*406dup	ENSP00000482149.2:n.*398_*406dup
ENST00000683378.1:n.504_512dup
ENST00000336642.9:c.312_320dup	ENSP00000338009.5:p.Arg106_Arg107insSerValArg
ENST00000345378.7:c.1281_1289dup	ENSP00000223366.2:p.Arg429_Arg430insSerValArg
ENST00000403799.8:c.1278_1286dup MANE Select	ENSP00000384247.3:p.Arg428_Arg429insSerValArg
ENST00000671824.1:c.1341_1349dup	ENSP00000500264.1:p.Arg449_Arg450insSerValArg
ENST00000672743.1:n.290_298dup
ENST00000673284.1:c.1278_1286dup	ENSP00000499852.1:p.Arg428_Arg429insSerValArg
ENST00000336642.8:c.330_338dup	ENSP00000338009.4:p.Arg112_Arg113insSerValArg
ENST00000345378.6:c.1281_1289dup	ENSP00000223366.2:p.Arg429_Arg430insSerValArg
ENST00000395796.7:c.1275_1283dup	ENSP00000379142.3:p.Arg427_Arg428insSerValArg
ENST00000403799.7:c.1278_1286dup	ENSP00000384247.3:p.Arg428_Arg429insSerValArg
ENST00000437084.1:c.1227_1235dup	ENSP00000402840.1:p.Arg411_Arg412insSerValArg
ENST00000459642.1:n.658_666dup
ENST00000616242.4:c.1275_1283dup	ENSP00000482149.1:p.Arg427_Arg428insSerValArg
NM_000162.3:c.1278_1286dup	NP_000153.1:p.Arg428_Arg429insSerValArg
NM_033507.1:c.1281_1289dup	NP_277042.1:p.Arg429_Arg430insSerValArg
NM_033508.1:c.1275_1283dup	NP_277043.1:p.Arg427_Arg428insSerValArg
NM_000162.4:c.1278_1286dup	NP_000153.1:p.Arg428_Arg429insSerValArg
NM_001354800.1:c.1278_1286dup	NP_001341729.1:p.Arg428_Arg429insSerValArg
NM_001354801.1:c.267_275dup	NP_001341730.1:p.Arg91_Arg92insSerValArg
NM_001354802.1:c.138_146dup	NP_001341731.1:p.Arg48_Arg49insSerValArg
NM_001354803.1:c.312_320dup	NP_001341732.1:p.Arg106_Arg107insSerValArg
NM_033507.2:c.1281_1289dup	NP_277042.1:p.Arg429_Arg430insSerValArg
NM_033508.2:c.1275_1283dup	NP_277043.1:p.Arg427_Arg428insSerValArg
XM_024446707.1:c.138_146dup	XP_024302475.1:p.Arg48_Arg49insSerValArg
NM_000162.5:c.1278_1286dup MANE Select	NP_000153.1:p.Arg428_Arg429insSerValArg
NM_033507.3:c.1281_1289dup	NP_277042.1:p.Arg429_Arg430insSerValArg
NM_033508.3:c.1275_1283dup	NP_277043.1:p.Arg427_Arg428insSerValArg
NM_001354803.2:c.312_320dup	NP_001341732.1:p.Arg106_Arg107insSerValArg