Canonical Allele Identifier: CA367398398

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44185138A>C (hg19) ; chr7:g.44145539A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145539A>C , CM000669.2:g.44145539A>C	GRCh38
NC_000007.13:g.44185138A>C , CM000669.1:g.44185138A>C	GRCh37
NC_000007.12:g.44151663A>C	NCBI36
NG_008847.1:g.48885T>G
NG_008847.2:g.57632T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1209T>G	ENSP00000379142.4:n.*1209T>G
ENST00000616242.5:c.*331T>G	ENSP00000482149.2:n.*331T>G
ENST00000683378.1:n.437T>G
ENST00000336642.9:c.245T>G	ENSP00000338009.5:p.Ile82Ser
ENST00000345378.7:c.1214T>G	ENSP00000223366.2:p.Ile405Ser
ENST00000403799.8:c.1211T>G MANE Select	ENSP00000384247.3:p.Ile404Ser
ENST00000671824.1:c.1274T>G	ENSP00000500264.1:p.Ile425Ser
ENST00000672743.1:n.223T>G
ENST00000673284.1:c.1211T>G	ENSP00000499852.1:p.Ile404Ser
ENST00000336642.8:c.263T>G	ENSP00000338009.4:p.Ile88Ser
ENST00000345378.6:c.1214T>G	ENSP00000223366.2:p.Ile405Ser
ENST00000395796.7:c.1208T>G	ENSP00000379142.3:p.Ile403Ser
ENST00000403799.7:c.1211T>G	ENSP00000384247.3:p.Ile404Ser
ENST00000437084.1:c.1160T>G	ENSP00000402840.1:p.Ile387Ser
ENST00000459642.1:n.591T>G
ENST00000616242.4:c.1208T>G	ENSP00000482149.1:p.Ile403Ser
NM_000162.3:c.1211T>G	NP_000153.1:p.Ile404Ser
NM_033507.1:c.1214T>G	NP_277042.1:p.Ile405Ser
NM_033508.1:c.1208T>G	NP_277043.1:p.Ile403Ser
NM_000162.4:c.1211T>G	NP_000153.1:p.Ile404Ser
NM_001354800.1:c.1211T>G	NP_001341729.1:p.Ile404Ser
NM_001354801.1:c.200T>G	NP_001341730.1:p.Ile67Ser
NM_001354802.1:c.71T>G	NP_001341731.1:p.Ile24Ser
NM_001354803.1:c.245T>G	NP_001341732.1:p.Ile82Ser
NM_033507.2:c.1214T>G	NP_277042.1:p.Ile405Ser
NM_033508.2:c.1208T>G	NP_277043.1:p.Ile403Ser
XM_024446707.1:c.71T>G	XP_024302475.1:p.Ile24Ser
NM_000162.5:c.1211T>G MANE Select	NP_000153.1:p.Ile404Ser
NM_033507.3:c.1214T>G	NP_277042.1:p.Ile405Ser
NM_033508.3:c.1208T>G	NP_277043.1:p.Ile403Ser
NM_001354803.2:c.245T>G	NP_001341732.1:p.Ile82Ser