Canonical Allele Identifier: CA454863218

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44185191C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145592C>G , CM000669.2:g.44145592C>G	GRCh38
NC_000007.13:g.44185191C>G , CM000669.1:g.44185191C>G	GRCh37
NC_000007.12:g.44151716C>G	NCBI36
NG_008847.1:g.48832G>C
NG_008847.2:g.57579G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1156G>C	ENSP00000379142.4:n.*1156G>C
ENST00000616242.5:c.*278G>C	ENSP00000482149.2:n.*278G>C
ENST00000683378.1:n.384G>C
ENST00000336642.9:c.192G>C	ENSP00000338009.5:p.Leu64=
ENST00000345378.7:c.1161G>C	ENSP00000223366.2:p.Leu387=
ENST00000403799.8:c.1158G>C MANE Select	ENSP00000384247.3:p.Leu386=
ENST00000671824.1:c.1221G>C	ENSP00000500264.1:p.Leu407=
ENST00000672743.1:n.170G>C
ENST00000673284.1:c.1158G>C	ENSP00000499852.1:p.Leu386=
ENST00000336642.8:c.210G>C	ENSP00000338009.4:p.Leu70=
ENST00000345378.6:c.1161G>C	ENSP00000223366.2:p.Leu387=
ENST00000395796.7:c.1155G>C	ENSP00000379142.3:p.Leu385=
ENST00000403799.7:c.1158G>C	ENSP00000384247.3:p.Leu386=
ENST00000437084.1:c.1107G>C	ENSP00000402840.1:p.Leu369=
ENST00000459642.1:n.538G>C
ENST00000616242.4:c.1155G>C	ENSP00000482149.1:p.Leu385=
NM_000162.3:c.1158G>C	NP_000153.1:p.Leu386=
NM_033507.1:c.1161G>C	NP_277042.1:p.Leu387=
NM_033508.1:c.1155G>C	NP_277043.1:p.Leu385=
NM_000162.4:c.1158G>C	NP_000153.1:p.Leu386=
NM_001354800.1:c.1158G>C	NP_001341729.1:p.Leu386=
NM_001354801.1:c.147G>C	NP_001341730.1:p.Leu49=
NM_001354802.1:c.18G>C	NP_001341731.1:p.Leu6=
NM_001354803.1:c.192G>C	NP_001341732.1:p.Leu64=
NM_033507.2:c.1161G>C	NP_277042.1:p.Leu387=
NM_033508.2:c.1155G>C	NP_277043.1:p.Leu385=
XM_024446707.1:c.18G>C	XP_024302475.1:p.Leu6=
NM_000162.5:c.1158G>C MANE Select	NP_000153.1:p.Leu386=
NM_033507.3:c.1161G>C	NP_277042.1:p.Leu387=
NM_033508.3:c.1155G>C	NP_277043.1:p.Leu385=
NM_001354803.2:c.192G>C	NP_001341732.1:p.Leu64=