Canonical Allele Identifier: CA367400596

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44187343A>C (hg19) ; chr7:g.44147744A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44147744A>C , CM000669.2:g.44147744A>C	GRCh38
NC_000007.13:g.44187343A>C , CM000669.1:g.44187343A>C	GRCh37
NC_000007.12:g.44153868A>C	NCBI36
NG_008847.1:g.46680T>G
NG_008847.2:g.55427T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*767T>G	ENSP00000379142.4:n.*767T>G
ENST00000616242.5:c.769T>G	ENSP00000482149.2:p.Trp257Gly
ENST00000345378.7:c.772T>G	ENSP00000223366.2:p.Trp258Gly
ENST00000403799.8:c.769T>G MANE Select	ENSP00000384247.3:p.Trp257Gly
ENST00000671824.1:c.769T>G	ENSP00000500264.1:p.Trp257Gly
ENST00000673284.1:c.769T>G	ENSP00000499852.1:p.Trp257Gly
ENST00000345378.6:c.772T>G	ENSP00000223366.2:p.Trp258Gly
ENST00000395796.7:c.766T>G	ENSP00000379142.3:p.Trp256Gly
ENST00000403799.7:c.769T>G	ENSP00000384247.3:p.Trp257Gly
ENST00000437084.1:c.718T>G	ENSP00000402840.1:p.Trp240Gly
ENST00000616242.4:c.766T>G	ENSP00000482149.1:p.Trp256Gly
NM_000162.3:c.769T>G	NP_000153.1:p.Trp257Gly
NM_033507.1:c.772T>G	NP_277042.1:p.Trp258Gly
NM_033508.1:c.766T>G	NP_277043.1:p.Trp256Gly
XR_927223.1:n.78A>C
NM_000162.4:c.769T>G	NP_000153.1:p.Trp257Gly
NM_001354800.1:c.769T>G	NP_001341729.1:p.Trp257Gly
NM_033507.2:c.772T>G	NP_277042.1:p.Trp258Gly
NM_033508.2:c.766T>G	NP_277043.1:p.Trp256Gly
XR_927223.2:n.78A>C
NM_000162.5:c.769T>G MANE Select	NP_000153.1:p.Trp257Gly
NM_033507.3:c.772T>G	NP_277042.1:p.Trp258Gly
NM_033508.3:c.766T>G	NP_277043.1:p.Trp256Gly