Canonical Allele Identifier: CA367398207

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44185100G>C (hg19) ; chr7:g.44145501G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145501G>C , CM000669.2:g.44145501G>C	GRCh38
NC_000007.13:g.44185100G>C , CM000669.1:g.44185100G>C	GRCh37
NC_000007.12:g.44151625G>C	NCBI36
NG_008847.1:g.48923C>G
NG_008847.2:g.57670C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1247C>G	ENSP00000379142.4:n.*1247C>G
ENST00000616242.5:c.*369C>G	ENSP00000482149.2:n.*369C>G
ENST00000683378.1:n.475C>G
ENST00000336642.9:c.283C>G	ENSP00000338009.5:p.Pro95Ala
ENST00000345378.7:c.1252C>G	ENSP00000223366.2:p.Pro418Ala
ENST00000403799.8:c.1249C>G MANE Select	ENSP00000384247.3:p.Pro417Ala
ENST00000671824.1:c.1312C>G	ENSP00000500264.1:p.Pro438Ala
ENST00000672743.1:n.261C>G
ENST00000673284.1:c.1249C>G	ENSP00000499852.1:p.Pro417Ala
ENST00000336642.8:c.301C>G	ENSP00000338009.4:p.Pro101Ala
ENST00000345378.6:c.1252C>G	ENSP00000223366.2:p.Pro418Ala
ENST00000395796.7:c.1246C>G	ENSP00000379142.3:p.Pro416Ala
ENST00000403799.7:c.1249C>G	ENSP00000384247.3:p.Pro417Ala
ENST00000437084.1:c.1198C>G	ENSP00000402840.1:p.Pro400Ala
ENST00000459642.1:n.629C>G
ENST00000616242.4:c.1246C>G	ENSP00000482149.1:p.Pro416Ala
NM_000162.3:c.1249C>G	NP_000153.1:p.Pro417Ala
NM_033507.1:c.1252C>G	NP_277042.1:p.Pro418Ala
NM_033508.1:c.1246C>G	NP_277043.1:p.Pro416Ala
NM_000162.4:c.1249C>G	NP_000153.1:p.Pro417Ala
NM_001354800.1:c.1249C>G	NP_001341729.1:p.Pro417Ala
NM_001354801.1:c.238C>G	NP_001341730.1:p.Pro80Ala
NM_001354802.1:c.109C>G	NP_001341731.1:p.Pro37Ala
NM_001354803.1:c.283C>G	NP_001341732.1:p.Pro95Ala
NM_033507.2:c.1252C>G	NP_277042.1:p.Pro418Ala
NM_033508.2:c.1246C>G	NP_277043.1:p.Pro416Ala
XM_024446707.1:c.109C>G	XP_024302475.1:p.Pro37Ala
NM_000162.5:c.1249C>G MANE Select	NP_000153.1:p.Pro417Ala
NM_033507.3:c.1252C>G	NP_277042.1:p.Pro418Ala
NM_033508.3:c.1246C>G	NP_277043.1:p.Pro416Ala
NM_001354803.2:c.283C>G	NP_001341732.1:p.Pro95Ala