Canonical Allele Identifier: CA1703613460

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44146479_44146480delinsCG , CM000669.2:g.44146479_44146480delinsCG	GRCh38
NC_000007.13:g.44186078_44186079delinsCG , CM000669.1:g.44186078_44186079delinsCG	GRCh37
NC_000007.12:g.44152603_44152604delinsCG	NCBI36
NG_008847.1:g.47944_47945delinsCG
NG_008847.2:g.56691_56692delinsCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*1000_*1001delinsCG	ENSP00000379142.4:n.*1000_*1001delinsCG
ENST00000616242.5:c.*122_*123delinsCG	ENSP00000482149.2:n.*122_*123delinsCG
ENST00000683378.1:n.228_229delinsCG
ENST00000345378.7:c.1005_1006delinsCG	ENSP00000223366.2:p.Phe335=
ENST00000403799.8:c.1002_1003delinsCG MANE Select	ENSP00000384247.3:p.Phe334=
ENST00000671824.1:c.1065_1066delinsCG	ENSP00000500264.1:p.Phe355=
ENST00000673284.1:c.1002_1003delinsCG	ENSP00000499852.1:p.Phe334=
ENST00000345378.6:c.1005_1006delinsCG	ENSP00000223366.2:p.Phe335=
ENST00000395796.7:c.999_1000delinsCG	ENSP00000379142.3:p.Phe333=
ENST00000403799.7:c.1002_1003delinsCG	ENSP00000384247.3:p.Phe334=
ENST00000437084.1:c.951_952delinsCG	ENSP00000402840.1:p.Phe317=
ENST00000473353.1:n.300_301delinsCG
ENST00000616242.4:c.999_1000delinsCG	ENSP00000482149.1:p.Phe333=
NM_000162.3:c.1002_1003delinsCG	NP_000153.1:p.Phe334=
NM_033507.1:c.1005_1006delinsCG	NP_277042.1:p.Phe335=
NM_033508.1:c.999_1000delinsCG	NP_277043.1:p.Phe333=
NM_000162.4:c.1002_1003delinsCG	NP_000153.1:p.Phe334=
NM_001354800.1:c.1002_1003delinsCG	NP_001341729.1:p.Phe334=
NM_001354801.1:c.8+139_8+140delinsCG	NP_001341730.1:n.8+139_8+140delinsCG
NM_033507.2:c.1005_1006delinsCG	NP_277042.1:p.Phe335=
NM_033508.2:c.999_1000delinsCG	NP_277043.1:p.Phe333=
NM_000162.5:c.1002_1003delinsCG MANE Select	NP_000153.1:p.Phe334=
NM_033507.3:c.1005_1006delinsCG	NP_277042.1:p.Phe335=
NM_033508.3:c.999_1000delinsCG	NP_277043.1:p.Phe333=