Canonical Allele Identifier: CA367398353

Gene: GCK

Linked Data

• gnomAD v4: 7-44145531-C-A
• MyVariant Identifiers: chr7:g.44185130C>A (hg19) ; chr7:g.44145531C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145531C>A , CM000669.2:g.44145531C>A	GRCh38
NC_000007.13:g.44185130C>A , CM000669.1:g.44185130C>A	GRCh37
NC_000007.12:g.44151655C>A	NCBI36
NG_008847.1:g.48893G>T
NG_008847.2:g.57640G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*1217G>T	ENSP00000379142.4:n.*1217G>T
ENST00000616242.5:c.*339G>T	ENSP00000482149.2:n.*339G>T
ENST00000683378.1:n.445G>T
ENST00000336642.9:c.253G>T	ENSP00000338009.5:p.Gly85Cys
ENST00000345378.7:c.1222G>T	ENSP00000223366.2:p.Gly408Cys
ENST00000403799.8:c.1219G>T MANE Select	ENSP00000384247.3:p.Gly407Cys
ENST00000671824.1:c.1282G>T	ENSP00000500264.1:p.Gly428Cys
ENST00000672743.1:n.231G>T
ENST00000673284.1:c.1219G>T	ENSP00000499852.1:p.Gly407Cys
ENST00000336642.8:c.271G>T	ENSP00000338009.4:p.Gly91Cys
ENST00000345378.6:c.1222G>T	ENSP00000223366.2:p.Gly408Cys
ENST00000395796.7:c.1216G>T	ENSP00000379142.3:p.Gly406Cys
ENST00000403799.7:c.1219G>T	ENSP00000384247.3:p.Gly407Cys
ENST00000437084.1:c.1168G>T	ENSP00000402840.1:p.Gly390Cys
ENST00000459642.1:n.599G>T
ENST00000616242.4:c.1216G>T	ENSP00000482149.1:p.Gly406Cys
NM_000162.3:c.1219G>T	NP_000153.1:p.Gly407Cys
NM_033507.1:c.1222G>T	NP_277042.1:p.Gly408Cys
NM_033508.1:c.1216G>T	NP_277043.1:p.Gly406Cys
NM_000162.4:c.1219G>T	NP_000153.1:p.Gly407Cys
NM_001354800.1:c.1219G>T	NP_001341729.1:p.Gly407Cys
NM_001354801.1:c.208G>T	NP_001341730.1:p.Gly70Cys
NM_001354802.1:c.79G>T	NP_001341731.1:p.Gly27Cys
NM_001354803.1:c.253G>T	NP_001341732.1:p.Gly85Cys
NM_033507.2:c.1222G>T	NP_277042.1:p.Gly408Cys
NM_033508.2:c.1216G>T	NP_277043.1:p.Gly406Cys
XM_024446707.1:c.79G>T	XP_024302475.1:p.Gly27Cys
NM_000162.5:c.1219G>T MANE Select	NP_000153.1:p.Gly407Cys
NM_033507.3:c.1222G>T	NP_277042.1:p.Gly408Cys
NM_033508.3:c.1216G>T	NP_277043.1:p.Gly406Cys
NM_001354803.2:c.253G>T	NP_001341732.1:p.Gly85Cys