Canonical Allele Identifier: CA367396734

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44184740G>A (hg19) ; chr7:g.44145141G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145141G>A , CM000669.2:g.44145141G>A	GRCh38
NC_000007.13:g.44184740G>A , CM000669.1:g.44184740G>A	GRCh37
NC_000007.12:g.44151265G>A	NCBI36
NG_008847.1:g.49283C>T
NG_008847.2:g.58030C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1391C>T	ENSP00000379142.4:n.*1391C>T
ENST00000616242.5:c.*513C>T	ENSP00000482149.2:n.*513C>T
ENST00000683378.1:n.619C>T
ENST00000336642.9:c.427C>T	ENSP00000338009.5:p.Gln143Ter
ENST00000345378.7:c.1396C>T	ENSP00000223366.2:p.Gln466Ter
ENST00000403799.8:c.1393C>T MANE Select	ENSP00000384247.3:p.Gln465Ter
ENST00000671824.1:c.1456C>T	ENSP00000500264.1:p.Gln486Ter
ENST00000672743.1:n.381+24C>T
ENST00000673284.1:c.1369+24C>T	ENSP00000499852.1:n.1369+24C>T
ENST00000336642.8:c.445C>T	ENSP00000338009.4:p.Gln149Ter
ENST00000345378.6:c.1396C>T	ENSP00000223366.2:p.Gln466Ter
ENST00000395796.7:c.1390C>T	ENSP00000379142.3:p.Gln464Ter
ENST00000403799.7:c.1393C>T	ENSP00000384247.3:p.Gln465Ter
ENST00000437084.1:c.1342C>T	ENSP00000402840.1:p.Gln448Ter
ENST00000459642.1:n.773C>T
ENST00000616242.4:c.1390C>T	ENSP00000482149.1:p.Gln464Ter
NM_000162.3:c.1393C>T	NP_000153.1:p.Gln465Ter
NM_033507.1:c.1396C>T	NP_277042.1:p.Gln466Ter
NM_033508.1:c.1390C>T	NP_277043.1:p.Gln464Ter
NM_000162.4:c.1393C>T	NP_000153.1:p.Gln465Ter
NM_001354800.1:c.1369+24C>T	NP_001341729.1:n.1369+24C>T
NM_001354801.1:c.382C>T	NP_001341730.1:p.Gln128Ter
NM_001354802.1:c.229+24C>T	NP_001341731.1:n.229+24C>T
NM_001354803.1:c.427C>T	NP_001341732.1:p.Gln143Ter
NM_033507.2:c.1396C>T	NP_277042.1:p.Gln466Ter
NM_033508.2:c.1390C>T	NP_277043.1:p.Gln464Ter
XM_024446707.1:c.253C>T	XP_024302475.1:p.Gln85Ter
NM_000162.5:c.1393C>T MANE Select	NP_000153.1:p.Gln465Ter
NM_033507.3:c.1396C>T	NP_277042.1:p.Gln466Ter
NM_033508.3:c.1390C>T	NP_277043.1:p.Gln464Ter
NM_001354803.2:c.427C>T	NP_001341732.1:p.Gln143Ter