Canonical Allele Identifier: CA2682580176

Gene: GCK

Linked Data

• gnomAD v4: 7-44145123-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145123G>T , CM000669.2:g.44145123G>T	GRCh38
NC_000007.13:g.44184722G>T , CM000669.1:g.44184722G>T	GRCh37
NC_000007.12:g.44151247G>T	NCBI36
NG_008847.1:g.49301C>A
NG_008847.2:g.58048C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1409C>A	ENSP00000379142.4:n.*1409C>A
ENST00000616242.5:c.*531C>A	ENSP00000482149.2:n.*531C>A
ENST00000683378.1:n.637C>A
ENST00000336642.9:c.*13C>A	ENSP00000338009.5:n.*13C>A
ENST00000345378.7:c.*13C>A	ENSP00000223366.2:n.*13C>A
ENST00000403799.8:c.*13C>A MANE Select	ENSP00000384247.3:n.*13C>A
ENST00000671824.1:c.*13C>A	ENSP00000500264.1:n.*13C>A
ENST00000672743.1:n.381+42C>A
ENST00000673284.1:c.1369+42C>A	ENSP00000499852.1:n.1369+42C>A
ENST00000336642.8:c.463C>A	ENSP00000338009.4:n.463C>A
ENST00000345378.6:c.*13C>A	ENSP00000223366.2:n.*13C>A
ENST00000395796.7:c.*13C>A	ENSP00000379142.3:n.*13C>A
ENST00000403799.7:c.*13C>A	ENSP00000384247.3:n.*13C>A
ENST00000459642.1:n.791C>A
ENST00000616242.4:c.1408C>A	ENSP00000482149.1:n.1408C>A
NM_000162.3:c.*13C>A	NP_000153.1:n.*13C>A
NM_033507.1:c.*13C>A	NP_277042.1:n.*13C>A
NM_033508.1:c.*13C>A	NP_277043.1:n.*13C>A
NM_000162.4:c.*13C>A	NP_000153.1:n.*13C>A
NM_001354800.1:c.1369+42C>A	NP_001341729.1:n.1369+42C>A
NM_001354801.1:c.*13C>A	NP_001341730.1:n.*13C>A
NM_001354802.1:c.229+42C>A	NP_001341731.1:n.229+42C>A
NM_001354803.1:c.*13C>A	NP_001341732.1:n.*13C>A
NM_033507.2:c.*13C>A	NP_277042.1:n.*13C>A
NM_033508.2:c.*13C>A	NP_277043.1:n.*13C>A
XM_024446707.1:c.*13C>A	XP_024302475.1:n.*13C>A
NM_000162.5:c.*13C>A MANE Select	NP_000153.1:n.*13C>A
NM_033507.3:c.*13C>A	NP_277042.1:n.*13C>A
NM_033508.3:c.*13C>A	NP_277043.1:n.*13C>A
NM_001354803.2:c.*13C>A	NP_001341732.1:n.*13C>A