Canonical Allele Identifier: CA367403544

Gene: GCK

Linked Data

• ClinVar Variation Id: 2682651
• ClinVar RCV Id: RCV003481518
• MyVariant Identifiers: chr7:g.44192998A>G (hg19) ; chr7:g.44153399A>G (hg38)
• ERepo: CA367403544/MONDO:0015967/086

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44153399A>G , CM000669.2:g.44153399A>G	GRCh38
NC_000007.13:g.44192998A>G , CM000669.1:g.44192998A>G	GRCh37
NC_000007.12:g.44159523A>G	NCBI36
NG_008847.1:g.41025T>C
NG_008847.2:g.49772T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*108T>C	ENSP00000379142.4:n.*108T>C
ENST00000616242.5:c.110T>C	ENSP00000482149.2:p.Met37Thr
ENST00000682635.1:n.596T>C
ENST00000345378.7:c.113T>C	ENSP00000223366.2:p.Met38Thr
ENST00000403799.8:c.110T>C MANE Select	ENSP00000384247.3:p.Met37Thr
ENST00000671824.1:c.110T>C	ENSP00000500264.1:p.Met37Thr
ENST00000673284.1:c.110T>C	ENSP00000499852.1:p.Met37Thr
ENST00000345378.6:c.113T>C	ENSP00000223366.2:p.Met38Thr
ENST00000395796.7:c.107T>C	ENSP00000379142.3:p.Met36Thr
ENST00000403799.7:c.110T>C	ENSP00000384247.3:p.Met37Thr
ENST00000437084.1:c.110T>C	ENSP00000402840.1:p.Met37Thr
ENST00000476008.1:n.545T>C
ENST00000616242.4:c.107T>C	ENSP00000482149.1:p.Met36Thr
NM_000162.3:c.110T>C	NP_000153.1:p.Met37Thr
NM_033507.1:c.113T>C	NP_277042.1:p.Met38Thr
NM_033508.1:c.107T>C	NP_277043.1:p.Met36Thr
NM_000162.4:c.110T>C	NP_000153.1:p.Met37Thr
NM_001354800.1:c.110T>C	NP_001341729.1:p.Met37Thr
NM_033507.2:c.113T>C	NP_277042.1:p.Met38Thr
NM_033508.2:c.107T>C	NP_277043.1:p.Met36Thr
NM_000162.5:c.110T>C MANE Select	NP_000153.1:p.Met37Thr
NM_033507.3:c.113T>C	NP_277042.1:p.Met38Thr
NM_033508.3:c.107T>C	NP_277043.1:p.Met36Thr