Canonical Allele Identifier: CA454606389

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44184792C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145193C>A , CM000669.2:g.44145193C>A	GRCh38
NC_000007.13:g.44184792C>A , CM000669.1:g.44184792C>A	GRCh37
NC_000007.12:g.44151317C>A	NCBI36
NG_008847.1:g.49231G>T
NG_008847.2:g.57978G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1339G>T	ENSP00000379142.4:n.*1339G>T
ENST00000616242.5:c.*461G>T	ENSP00000482149.2:n.*461G>T
ENST00000683378.1:n.567G>T
ENST00000336642.9:c.375G>T	ENSP00000338009.5:p.Arg125=
ENST00000345378.7:c.1344G>T	ENSP00000223366.2:p.Arg448=
ENST00000403799.8:c.1341G>T MANE Select	ENSP00000384247.3:p.Arg447=
ENST00000671824.1:c.1404G>T	ENSP00000500264.1:p.Arg468=
ENST00000672743.1:n.353G>T
ENST00000673284.1:c.1341G>T	ENSP00000499852.1:p.Arg447=
ENST00000336642.8:c.393G>T	ENSP00000338009.4:p.Arg131=
ENST00000345378.6:c.1344G>T	ENSP00000223366.2:p.Arg448=
ENST00000395796.7:c.1338G>T	ENSP00000379142.3:p.Arg446=
ENST00000403799.7:c.1341G>T	ENSP00000384247.3:p.Arg447=
ENST00000437084.1:c.1290G>T	ENSP00000402840.1:p.Arg430=
ENST00000459642.1:n.721G>T
ENST00000616242.4:c.1338G>T	ENSP00000482149.1:p.Arg446=
NM_000162.3:c.1341G>T	NP_000153.1:p.Arg447=
NM_033507.1:c.1344G>T	NP_277042.1:p.Arg448=
NM_033508.1:c.1338G>T	NP_277043.1:p.Arg446=
NM_000162.4:c.1341G>T	NP_000153.1:p.Arg447=
NM_001354800.1:c.1341G>T	NP_001341729.1:p.Arg447=
NM_001354801.1:c.330G>T	NP_001341730.1:p.Arg110=
NM_001354802.1:c.201G>T	NP_001341731.1:p.Arg67=
NM_001354803.1:c.375G>T	NP_001341732.1:p.Arg125=
NM_033507.2:c.1344G>T	NP_277042.1:p.Arg448=
NM_033508.2:c.1338G>T	NP_277043.1:p.Arg446=
XM_024446707.1:c.201G>T	XP_024302475.1:p.Arg67=
NM_000162.5:c.1341G>T MANE Select	NP_000153.1:p.Arg447=
NM_033507.3:c.1344G>T	NP_277042.1:p.Arg448=
NM_033508.3:c.1338G>T	NP_277043.1:p.Arg446=
NM_001354803.2:c.375G>T	NP_001341732.1:p.Arg125=