Canonical Allele Identifier: CA2839409320

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44152246C>A , CM000669.2:g.44152246C>A	GRCh38
NC_000007.13:g.44191845C>A , CM000669.1:g.44191845C>A	GRCh37
NC_000007.12:g.44158370C>A	NCBI36
NG_008847.1:g.42178G>T
NG_008847.2:g.50925G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*361+25G>T	ENSP00000379142.4:n.*361+25G>T
ENST00000616242.5:c.363+25G>T	ENSP00000482149.2:n.363+25G>T
ENST00000682635.1:n.849+25G>T
ENST00000345378.7:c.366+25G>T	ENSP00000223366.2:n.366+25G>T
ENST00000403799.8:c.363+25G>T MANE Select	ENSP00000384247.3:n.363+25G>T
ENST00000671824.1:c.363+25G>T	ENSP00000500264.1:n.363+25G>T
ENST00000673284.1:c.363+25G>T	ENSP00000499852.1:n.363+25G>T
ENST00000345378.6:c.366+25G>T	ENSP00000223366.2:n.366+25G>T
ENST00000395796.7:c.360+25G>T	ENSP00000379142.3:n.360+25G>T
ENST00000403799.7:c.363+25G>T	ENSP00000384247.3:n.363+25G>T
ENST00000437084.1:c.363+25G>T	ENSP00000402840.1:n.363+25G>T
ENST00000616242.4:c.360+25G>T	ENSP00000482149.1:n.360+25G>T
NM_000162.3:c.363+25G>T	NP_000153.1:n.363+25G>T
NM_033507.1:c.366+25G>T	NP_277042.1:n.366+25G>T
NM_033508.1:c.360+25G>T	NP_277043.1:n.360+25G>T
NM_000162.4:c.363+25G>T	NP_000153.1:n.363+25G>T
NM_001354800.1:c.363+25G>T	NP_001341729.1:n.363+25G>T
NM_033507.2:c.366+25G>T	NP_277042.1:n.366+25G>T
NM_033508.2:c.360+25G>T	NP_277043.1:n.360+25G>T
NM_000162.5:c.363+25G>T MANE Select	NP_000153.1:n.363+25G>T
NM_033507.3:c.366+25G>T	NP_277042.1:n.366+25G>T
NM_033508.3:c.360+25G>T	NP_277043.1:n.360+25G>T