Canonical Allele Identifier: CA367401371

Gene: GCK

Linked Data

• gnomAD v4: 7-44149832-C-T
• MyVariant Identifiers: chr7:g.44189431C>T (hg19) ; chr7:g.44149832C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44149832C>T , CM000669.2:g.44149832C>T	GRCh38
NC_000007.13:g.44189431C>T , CM000669.1:g.44189431C>T	GRCh37
NC_000007.12:g.44155956C>T	NCBI36
NG_008847.1:g.44592G>A
NG_008847.2:g.53339G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*605G>A	ENSP00000379142.4:n.*605G>A
ENST00000616242.5:c.607G>A	ENSP00000482149.2:p.Val203Met
ENST00000682635.1:n.1093G>A
ENST00000345378.7:c.610G>A	ENSP00000223366.2:p.Val204Met
ENST00000403799.8:c.607G>A MANE Select	ENSP00000384247.3:p.Val203Met
ENST00000671824.1:c.607G>A	ENSP00000500264.1:p.Val203Met
ENST00000673284.1:c.607G>A	ENSP00000499852.1:p.Val203Met
ENST00000345378.6:c.610G>A	ENSP00000223366.2:p.Val204Met
ENST00000395796.7:c.604G>A	ENSP00000379142.3:p.Val202Met
ENST00000403799.7:c.607G>A	ENSP00000384247.3:p.Val203Met
ENST00000437084.1:c.556G>A	ENSP00000402840.1:p.Val186Met
ENST00000616242.4:c.604G>A	ENSP00000482149.1:p.Val202Met
NM_000162.3:c.607G>A	NP_000153.1:p.Val203Met
NM_033507.1:c.610G>A	NP_277042.1:p.Val204Met
NM_033508.1:c.604G>A	NP_277043.1:p.Val202Met
NM_000162.4:c.607G>A	NP_000153.1:p.Val203Met
NM_001354800.1:c.607G>A	NP_001341729.1:p.Val203Met
NM_033507.2:c.610G>A	NP_277042.1:p.Val204Met
NM_033508.2:c.604G>A	NP_277043.1:p.Val202Met
NM_000162.5:c.607G>A MANE Select	NP_000153.1:p.Val203Met
NM_033507.3:c.610G>A	NP_277042.1:p.Val204Met
NM_033508.3:c.604G>A	NP_277043.1:p.Val202Met