Canonical Allele Identifier: CA367402699

Gene: GCK

Linked Data

• gnomAD v4: 7-44152314-A-G
• MyVariant Identifiers: chr7:g.44191913A>G (hg19) ; chr7:g.44152314A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44152314A>G , CM000669.2:g.44152314A>G	GRCh38
NC_000007.13:g.44191913A>G , CM000669.1:g.44191913A>G	GRCh37
NC_000007.12:g.44158438A>G	NCBI36
NG_008847.1:g.42110T>C
NG_008847.2:g.50857T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*318T>C	ENSP00000379142.4:n.*318T>C
ENST00000616242.5:c.320T>C	ENSP00000482149.2:p.Met107Thr
ENST00000682635.1:n.806T>C
ENST00000345378.7:c.323T>C	ENSP00000223366.2:p.Met108Thr
ENST00000403799.8:c.320T>C MANE Select	ENSP00000384247.3:p.Met107Thr
ENST00000671824.1:c.320T>C	ENSP00000500264.1:p.Met107Thr
ENST00000673284.1:c.320T>C	ENSP00000499852.1:p.Met107Thr
ENST00000345378.6:c.323T>C	ENSP00000223366.2:p.Met108Thr
ENST00000395796.7:c.317T>C	ENSP00000379142.3:p.Met106Thr
ENST00000403799.7:c.320T>C	ENSP00000384247.3:p.Met107Thr
ENST00000437084.1:c.320T>C	ENSP00000402840.1:p.Met107Thr
ENST00000616242.4:c.317T>C	ENSP00000482149.1:p.Met106Thr
NM_000162.3:c.320T>C	NP_000153.1:p.Met107Thr
NM_033507.1:c.323T>C	NP_277042.1:p.Met108Thr
NM_033508.1:c.317T>C	NP_277043.1:p.Met106Thr
NM_000162.4:c.320T>C	NP_000153.1:p.Met107Thr
NM_001354800.1:c.320T>C	NP_001341729.1:p.Met107Thr
NM_033507.2:c.323T>C	NP_277042.1:p.Met108Thr
NM_033508.2:c.317T>C	NP_277043.1:p.Met106Thr
NM_000162.5:c.320T>C MANE Select	NP_000153.1:p.Met107Thr
NM_033507.3:c.323T>C	NP_277042.1:p.Met108Thr
NM_033508.3:c.317T>C	NP_277043.1:p.Met106Thr