Canonical Allele Identifier: CA1703613457

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44146470C= , CM000669.2:g.44146470C=	GRCh38
NC_000007.13:g.44186069C= , CM000669.1:g.44186069C=	GRCh37
NC_000007.12:g.44152594C=	NCBI36
NG_008847.1:g.47954G=
NG_008847.2:g.56701G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1010G=	ENSP00000379142.4:n.*1010G=
ENST00000616242.5:c.*132G=	ENSP00000482149.2:n.*132G=
ENST00000683378.1:n.238G=
ENST00000345378.7:c.1015G=	ENSP00000223366.2:p.Val339=
ENST00000403799.8:c.1012G= MANE Select	ENSP00000384247.3:p.Val338=
ENST00000671824.1:c.1075G=	ENSP00000500264.1:p.Val359=
ENST00000673284.1:c.1012G=	ENSP00000499852.1:p.Val338=
ENST00000345378.6:c.1015G=	ENSP00000223366.2:p.Val339=
ENST00000395796.7:c.1009G=	ENSP00000379142.3:p.Val337=
ENST00000403799.7:c.1012G=	ENSP00000384247.3:p.Val338=
ENST00000437084.1:c.961G=	ENSP00000402840.1:p.Val321=
ENST00000473353.1:n.310G=
ENST00000616242.4:c.1009G=	ENSP00000482149.1:p.Val337=
NM_000162.3:c.1012G=	NP_000153.1:p.Val338=
NM_033507.1:c.1015G=	NP_277042.1:p.Val339=
NM_033508.1:c.1009G=	NP_277043.1:p.Val337=
NM_000162.4:c.1012G=	NP_000153.1:p.Val338=
NM_001354800.1:c.1012G=	NP_001341729.1:p.Val338=
NM_001354801.1:c.8+149G=	NP_001341730.1:n.8+149G=
NM_033507.2:c.1015G=	NP_277042.1:p.Val339=
NM_033508.2:c.1009G=	NP_277043.1:p.Val337=
NM_000162.5:c.1012G= MANE Select	NP_000153.1:p.Val338=
NM_033507.3:c.1015G=	NP_277042.1:p.Val339=
NM_033508.3:c.1009G=	NP_277043.1:p.Val337=