Canonical Allele Identifier: CA454606708

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44184867C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145268C>T , CM000669.2:g.44145268C>T	GRCh38
NC_000007.13:g.44184867C>T , CM000669.1:g.44184867C>T	GRCh37
NC_000007.12:g.44151392C>T	NCBI36
NG_008847.1:g.49156G>A
NG_008847.2:g.57903G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1264G>A	ENSP00000379142.4:n.*1264G>A
ENST00000616242.5:c.*386G>A	ENSP00000482149.2:n.*386G>A
ENST00000683378.1:n.492G>A
ENST00000336642.9:c.300G>A	ENSP00000338009.5:p.Arg100=
ENST00000345378.7:c.1269G>A	ENSP00000223366.2:p.Arg423=
ENST00000403799.8:c.1266G>A MANE Select	ENSP00000384247.3:p.Arg422=
ENST00000671824.1:c.1329G>A	ENSP00000500264.1:p.Arg443=
ENST00000672743.1:n.278G>A
ENST00000673284.1:c.1266G>A	ENSP00000499852.1:p.Arg422=
ENST00000336642.8:c.318G>A	ENSP00000338009.4:p.Arg106=
ENST00000345378.6:c.1269G>A	ENSP00000223366.2:p.Arg423=
ENST00000395796.7:c.1263G>A	ENSP00000379142.3:p.Arg421=
ENST00000403799.7:c.1266G>A	ENSP00000384247.3:p.Arg422=
ENST00000437084.1:c.1215G>A	ENSP00000402840.1:p.Arg405=
ENST00000459642.1:n.646G>A
ENST00000616242.4:c.1263G>A	ENSP00000482149.1:p.Arg421=
NM_000162.3:c.1266G>A	NP_000153.1:p.Arg422=
NM_033507.1:c.1269G>A	NP_277042.1:p.Arg423=
NM_033508.1:c.1263G>A	NP_277043.1:p.Arg421=
NM_000162.4:c.1266G>A	NP_000153.1:p.Arg422=
NM_001354800.1:c.1266G>A	NP_001341729.1:p.Arg422=
NM_001354801.1:c.255G>A	NP_001341730.1:p.Arg85=
NM_001354802.1:c.126G>A	NP_001341731.1:p.Arg42=
NM_001354803.1:c.300G>A	NP_001341732.1:p.Arg100=
NM_033507.2:c.1269G>A	NP_277042.1:p.Arg423=
NM_033508.2:c.1263G>A	NP_277043.1:p.Arg421=
XM_024446707.1:c.126G>A	XP_024302475.1:p.Arg42=
NM_000162.5:c.1266G>A MANE Select	NP_000153.1:p.Arg422=
NM_033507.3:c.1269G>A	NP_277042.1:p.Arg423=
NM_033508.3:c.1263G>A	NP_277043.1:p.Arg421=
NM_001354803.2:c.300G>A	NP_001341732.1:p.Arg100=