Canonical Allele Identifier: CA367403578

Gene: GCK

Linked Data

• dbSNP Id: rs1461524859
• gnomAD v2: 7-44193004-C-T
• MyVariant Identifiers: chr7:g.44193004C>T (hg19) ; chr7:g.44153405C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44153405C>T , CM000669.2:g.44153405C>T	GRCh38
NC_000007.13:g.44193004C>T , CM000669.1:g.44193004C>T	GRCh37
NC_000007.12:g.44159529C>T	NCBI36
NG_008847.1:g.41019G>A
NG_008847.2:g.49766G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*102G>A	ENSP00000379142.4:n.*102G>A
ENST00000616242.5:c.104G>A	ENSP00000482149.2:p.Arg35Lys
ENST00000682635.1:n.590G>A
ENST00000345378.7:c.107G>A	ENSP00000223366.2:p.Arg36Lys
ENST00000403799.8:c.104G>A MANE Select	ENSP00000384247.3:p.Arg35Lys
ENST00000671824.1:c.104G>A	ENSP00000500264.1:p.Arg35Lys
ENST00000673284.1:c.104G>A	ENSP00000499852.1:p.Arg35Lys
ENST00000345378.6:c.107G>A	ENSP00000223366.2:p.Arg36Lys
ENST00000395796.7:c.101G>A	ENSP00000379142.3:p.Arg34Lys
ENST00000403799.7:c.104G>A	ENSP00000384247.3:p.Arg35Lys
ENST00000437084.1:c.104G>A	ENSP00000402840.1:p.Arg35Lys
ENST00000476008.1:n.539G>A
ENST00000616242.4:c.101G>A	ENSP00000482149.1:p.Arg34Lys
NM_000162.3:c.104G>A	NP_000153.1:p.Arg35Lys
NM_033507.1:c.107G>A	NP_277042.1:p.Arg36Lys
NM_033508.1:c.101G>A	NP_277043.1:p.Arg34Lys
NM_000162.4:c.104G>A	NP_000153.1:p.Arg35Lys
NM_001354800.1:c.104G>A	NP_001341729.1:p.Arg35Lys
NM_033507.2:c.107G>A	NP_277042.1:p.Arg36Lys
NM_033508.2:c.101G>A	NP_277043.1:p.Arg34Lys
NM_000162.5:c.104G>A MANE Select	NP_000153.1:p.Arg35Lys
NM_033507.3:c.107G>A	NP_277042.1:p.Arg36Lys
NM_033508.3:c.101G>A	NP_277043.1:p.Arg34Lys