Canonical Allele Identifier: CA367396976

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44184802C>A (hg19) ; chr7:g.44145203C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145203C>A , CM000669.2:g.44145203C>A	GRCh38
NC_000007.13:g.44184802C>A , CM000669.1:g.44184802C>A	GRCh37
NC_000007.12:g.44151327C>A	NCBI36
NG_008847.1:g.49221G>T
NG_008847.2:g.57968G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1329G>T	ENSP00000379142.4:n.*1329G>T
ENST00000616242.5:c.*451G>T	ENSP00000482149.2:n.*451G>T
ENST00000683378.1:n.557G>T
ENST00000336642.9:c.365G>T	ENSP00000338009.5:p.Gly122Val
ENST00000345378.7:c.1334G>T	ENSP00000223366.2:p.Gly445Val
ENST00000403799.8:c.1331G>T MANE Select	ENSP00000384247.3:p.Gly444Val
ENST00000671824.1:c.1394G>T	ENSP00000500264.1:p.Gly465Val
ENST00000672743.1:n.343G>T
ENST00000673284.1:c.1331G>T	ENSP00000499852.1:p.Gly444Val
ENST00000336642.8:c.383G>T	ENSP00000338009.4:p.Gly128Val
ENST00000345378.6:c.1334G>T	ENSP00000223366.2:p.Gly445Val
ENST00000395796.7:c.1328G>T	ENSP00000379142.3:p.Gly443Val
ENST00000403799.7:c.1331G>T	ENSP00000384247.3:p.Gly444Val
ENST00000437084.1:c.1280G>T	ENSP00000402840.1:p.Gly427Val
ENST00000459642.1:n.711G>T
ENST00000616242.4:c.1328G>T	ENSP00000482149.1:p.Gly443Val
NM_000162.3:c.1331G>T	NP_000153.1:p.Gly444Val
NM_033507.1:c.1334G>T	NP_277042.1:p.Gly445Val
NM_033508.1:c.1328G>T	NP_277043.1:p.Gly443Val
NM_000162.4:c.1331G>T	NP_000153.1:p.Gly444Val
NM_001354800.1:c.1331G>T	NP_001341729.1:p.Gly444Val
NM_001354801.1:c.320G>T	NP_001341730.1:p.Gly107Val
NM_001354802.1:c.191G>T	NP_001341731.1:p.Gly64Val
NM_001354803.1:c.365G>T	NP_001341732.1:p.Gly122Val
NM_033507.2:c.1334G>T	NP_277042.1:p.Gly445Val
NM_033508.2:c.1328G>T	NP_277043.1:p.Gly443Val
XM_024446707.1:c.191G>T	XP_024302475.1:p.Gly64Val
NM_000162.5:c.1331G>T MANE Select	NP_000153.1:p.Gly444Val
NM_033507.3:c.1334G>T	NP_277042.1:p.Gly445Val
NM_033508.3:c.1328G>T	NP_277043.1:p.Gly443Val
NM_001354803.2:c.365G>T	NP_001341732.1:p.Gly122Val