Canonical Allele Identifier: CA1703612659

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145176G= , CM000669.2:g.44145176G=	GRCh38
NC_000007.13:g.44184775G= , CM000669.1:g.44184775G=	GRCh37
NC_000007.12:g.44151300G=	NCBI36
NG_008847.1:g.49248C=
NG_008847.2:g.57995C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1356C=	ENSP00000379142.4:n.*1356C=
ENST00000616242.5:c.*478C=	ENSP00000482149.2:n.*478C=
ENST00000683378.1:n.584C=
ENST00000336642.9:c.392C=	ENSP00000338009.5:p.Ser131=
ENST00000345378.7:c.1361C=	ENSP00000223366.2:p.Ser454=
ENST00000403799.8:c.1358C= MANE Select	ENSP00000384247.3:p.Ser453=
ENST00000671824.1:c.1421C=	ENSP00000500264.1:p.Ser474=
ENST00000672743.1:n.370C=
ENST00000673284.1:c.1358C=	ENSP00000499852.1:p.Ser453=
ENST00000336642.8:c.410C=	ENSP00000338009.4:p.Ser137=
ENST00000345378.6:c.1361C=	ENSP00000223366.2:p.Ser454=
ENST00000395796.7:c.1355C=	ENSP00000379142.3:p.Ser452=
ENST00000403799.7:c.1358C=	ENSP00000384247.3:p.Ser453=
ENST00000437084.1:c.1307C=	ENSP00000402840.1:p.Ser436=
ENST00000459642.1:n.738C=
ENST00000616242.4:c.1355C=	ENSP00000482149.1:p.Ser452=
NM_000162.3:c.1358C=	NP_000153.1:p.Ser453=
NM_033507.1:c.1361C=	NP_277042.1:p.Ser454=
NM_033508.1:c.1355C=	NP_277043.1:p.Ser452=
NM_000162.4:c.1358C=	NP_000153.1:p.Ser453=
NM_001354800.1:c.1358C=	NP_001341729.1:p.Ser453=
NM_001354801.1:c.347C=	NP_001341730.1:p.Ser116=
NM_001354802.1:c.218C=	NP_001341731.1:p.Ser73=
NM_001354803.1:c.392C=	NP_001341732.1:p.Ser131=
NM_033507.2:c.1361C=	NP_277042.1:p.Ser454=
NM_033508.2:c.1355C=	NP_277043.1:p.Ser452=
XM_024446707.1:c.218C=	XP_024302475.1:p.Ser73=
NM_000162.5:c.1358C= MANE Select	NP_000153.1:p.Ser453=
NM_033507.3:c.1361C=	NP_277042.1:p.Ser454=
NM_033508.3:c.1355C=	NP_277043.1:p.Ser452=
NM_001354803.2:c.392C=	NP_001341732.1:p.Ser131=