Canonical Allele Identifier: CA367396827

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44184761T>G (hg19) ; chr7:g.44145162T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145162T>G , CM000669.2:g.44145162T>G	GRCh38
NC_000007.13:g.44184761T>G , CM000669.1:g.44184761T>G	GRCh37
NC_000007.12:g.44151286T>G	NCBI36
NG_008847.1:g.49262A>C
NG_008847.2:g.58009A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*1370A>C	ENSP00000379142.4:n.*1370A>C
ENST00000616242.5:c.*492A>C	ENSP00000482149.2:n.*492A>C
ENST00000683378.1:n.598A>C
ENST00000336642.9:c.406A>C	ENSP00000338009.5:p.Lys136Gln
ENST00000345378.7:c.1375A>C	ENSP00000223366.2:p.Lys459Gln
ENST00000403799.8:c.1372A>C MANE Select	ENSP00000384247.3:p.Lys458Gln
ENST00000671824.1:c.1435A>C	ENSP00000500264.1:p.Lys479Gln
ENST00000672743.1:n.381+3A>C
ENST00000673284.1:c.1369+3A>C	ENSP00000499852.1:n.1369+3A>C
ENST00000336642.8:c.424A>C	ENSP00000338009.4:p.Lys142Gln
ENST00000345378.6:c.1375A>C	ENSP00000223366.2:p.Lys459Gln
ENST00000395796.7:c.1369A>C	ENSP00000379142.3:p.Lys457Gln
ENST00000403799.7:c.1372A>C	ENSP00000384247.3:p.Lys458Gln
ENST00000437084.1:c.1321A>C	ENSP00000402840.1:p.Lys441Gln
ENST00000459642.1:n.752A>C
ENST00000616242.4:c.1369A>C	ENSP00000482149.1:p.Lys457Gln
NM_000162.3:c.1372A>C	NP_000153.1:p.Lys458Gln
NM_033507.1:c.1375A>C	NP_277042.1:p.Lys459Gln
NM_033508.1:c.1369A>C	NP_277043.1:p.Lys457Gln
NM_000162.4:c.1372A>C	NP_000153.1:p.Lys458Gln
NM_001354800.1:c.1369+3A>C	NP_001341729.1:n.1369+3A>C
NM_001354801.1:c.361A>C	NP_001341730.1:p.Lys121Gln
NM_001354802.1:c.229+3A>C	NP_001341731.1:n.229+3A>C
NM_001354803.1:c.406A>C	NP_001341732.1:p.Lys136Gln
NM_033507.2:c.1375A>C	NP_277042.1:p.Lys459Gln
NM_033508.2:c.1369A>C	NP_277043.1:p.Lys457Gln
XM_024446707.1:c.232A>C	XP_024302475.1:p.Lys78Gln
NM_000162.5:c.1372A>C MANE Select	NP_000153.1:p.Lys458Gln
NM_033507.3:c.1375A>C	NP_277042.1:p.Lys459Gln
NM_033508.3:c.1369A>C	NP_277043.1:p.Lys457Gln
NM_001354803.2:c.406A>C	NP_001341732.1:p.Lys136Gln