Canonical Allele Identifier: CA367398987

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44185249A>C (hg19) ; chr7:g.44145650A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145650A>C , CM000669.2:g.44145650A>C	GRCh38
NC_000007.13:g.44185249A>C , CM000669.1:g.44185249A>C	GRCh37
NC_000007.12:g.44151774A>C	NCBI36
NG_008847.1:g.48774T>G
NG_008847.2:g.57521T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1098T>G	ENSP00000379142.4:n.*1098T>G
ENST00000616242.5:c.*220T>G	ENSP00000482149.2:n.*220T>G
ENST00000683378.1:n.326T>G
ENST00000336642.9:c.134T>G	ENSP00000338009.5:p.Val45Gly
ENST00000345378.7:c.1103T>G	ENSP00000223366.2:p.Val368Gly
ENST00000403799.8:c.1100T>G MANE Select	ENSP00000384247.3:p.Val367Gly
ENST00000671824.1:c.1163T>G	ENSP00000500264.1:p.Val388Gly
ENST00000672743.1:n.112T>G
ENST00000673284.1:c.1100T>G	ENSP00000499852.1:p.Val367Gly
ENST00000336642.8:c.152T>G	ENSP00000338009.4:p.Val51Gly
ENST00000345378.6:c.1103T>G	ENSP00000223366.2:p.Val368Gly
ENST00000395796.7:c.1097T>G	ENSP00000379142.3:p.Val366Gly
ENST00000403799.7:c.1100T>G	ENSP00000384247.3:p.Val367Gly
ENST00000437084.1:c.1049T>G	ENSP00000402840.1:p.Val350Gly
ENST00000459642.1:n.480T>G
ENST00000473353.1:n.398T>G
ENST00000616242.4:c.1097T>G	ENSP00000482149.1:p.Val366Gly
NM_000162.3:c.1100T>G	NP_000153.1:p.Val367Gly
NM_033507.1:c.1103T>G	NP_277042.1:p.Val368Gly
NM_033508.1:c.1097T>G	NP_277043.1:p.Val366Gly
NM_000162.4:c.1100T>G	NP_000153.1:p.Val367Gly
NM_001354800.1:c.1100T>G	NP_001341729.1:p.Val367Gly
NM_001354801.1:c.89T>G	NP_001341730.1:p.Val30Gly
NM_001354802.1:c.-41T>G	NP_001341731.1:n.-41T>G
NM_001354803.1:c.134T>G	NP_001341732.1:p.Val45Gly
NM_033507.2:c.1103T>G	NP_277042.1:p.Val368Gly
NM_033508.2:c.1097T>G	NP_277043.1:p.Val366Gly
XM_024446707.1:c.-41T>G	XP_024302475.1:n.-41T>G
NM_000162.5:c.1100T>G MANE Select	NP_000153.1:p.Val367Gly
NM_033507.3:c.1103T>G	NP_277042.1:p.Val368Gly
NM_033508.3:c.1097T>G	NP_277043.1:p.Val366Gly
NM_001354803.2:c.134T>G	NP_001341732.1:p.Val45Gly