Canonical Allele Identifier: CA574226451

Gene: GCK

Linked Data

• dbSNP Id: rs181540630
• gnomAD v2: 7-44186258-G-T
• gnomAD v4: 7-44146659-G-T
• MyVariant Identifiers: chr7:g.44186258G>T (hg19) ; chr7:g.44146659G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44146659G>T , CM000669.2:g.44146659G>T	GRCh38
NC_000007.13:g.44186258G>T , CM000669.1:g.44186258G>T	GRCh37
NC_000007.12:g.44152783G>T	NCBI36
NG_008847.1:g.47765C>A
NG_008847.2:g.56512C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*862-41C>A	ENSP00000379142.4:n.*862-41C>A
ENST00000616242.5:c.854-41C>A	ENSP00000482149.2:n.854-41C>A
ENST00000683378.1:n.49C>A
ENST00000345378.7:c.867-41C>A	ENSP00000223366.2:n.867-41C>A
ENST00000403799.8:c.864-41C>A MANE Select	ENSP00000384247.3:n.864-41C>A
ENST00000671824.1:c.927-41C>A	ENSP00000500264.1:n.927-41C>A
ENST00000673284.1:c.864-41C>A	ENSP00000499852.1:n.864-41C>A
ENST00000345378.6:c.867-41C>A	ENSP00000223366.2:n.867-41C>A
ENST00000395796.7:c.861-41C>A	ENSP00000379142.3:n.861-41C>A
ENST00000403799.7:c.864-41C>A	ENSP00000384247.3:n.864-41C>A
ENST00000437084.1:c.813-41C>A	ENSP00000402840.1:n.813-41C>A
ENST00000473353.1:n.162-41C>A
ENST00000616242.4:c.861-41C>A	ENSP00000482149.1:n.861-41C>A
NM_000162.3:c.864-41C>A	NP_000153.1:n.864-41C>A
NM_033507.1:c.867-41C>A	NP_277042.1:n.867-41C>A
NM_033508.1:c.861-41C>A	NP_277043.1:n.861-41C>A
NM_000162.4:c.864-41C>A	NP_000153.1:n.864-41C>A
NM_001354800.1:c.864-41C>A	NP_001341729.1:n.864-41C>A
NM_033507.2:c.867-41C>A	NP_277042.1:n.867-41C>A
NM_033508.2:c.861-41C>A	NP_277043.1:n.861-41C>A
NM_000162.5:c.864-41C>A MANE Select	NP_000153.1:n.864-41C>A
NM_033507.3:c.867-41C>A	NP_277042.1:n.867-41C>A
NM_033508.3:c.861-41C>A	NP_277043.1:n.861-41C>A