Canonical Allele Identifier: CA454607734

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44186076C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44146477C>G , CM000669.2:g.44146477C>G	GRCh38
NC_000007.13:g.44186076C>G , CM000669.1:g.44186076C>G	GRCh37
NC_000007.12:g.44152601C>G	NCBI36
NG_008847.1:g.47947G>C
NG_008847.2:g.56694G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1003G>C	ENSP00000379142.4:n.*1003G>C
ENST00000616242.5:c.*125G>C	ENSP00000482149.2:n.*125G>C
ENST00000683378.1:n.231G>C
ENST00000345378.7:c.1008G>C	ENSP00000223366.2:p.Val336=
ENST00000403799.8:c.1005G>C MANE Select	ENSP00000384247.3:p.Val335=
ENST00000671824.1:c.1068G>C	ENSP00000500264.1:p.Val356=
ENST00000673284.1:c.1005G>C	ENSP00000499852.1:p.Val335=
ENST00000345378.6:c.1008G>C	ENSP00000223366.2:p.Val336=
ENST00000395796.7:c.1002G>C	ENSP00000379142.3:p.Val334=
ENST00000403799.7:c.1005G>C	ENSP00000384247.3:p.Val335=
ENST00000437084.1:c.954G>C	ENSP00000402840.1:p.Val318=
ENST00000473353.1:n.303G>C
ENST00000616242.4:c.1002G>C	ENSP00000482149.1:p.Val334=
NM_000162.3:c.1005G>C	NP_000153.1:p.Val335=
NM_033507.1:c.1008G>C	NP_277042.1:p.Val336=
NM_033508.1:c.1002G>C	NP_277043.1:p.Val334=
NM_000162.4:c.1005G>C	NP_000153.1:p.Val335=
NM_001354800.1:c.1005G>C	NP_001341729.1:p.Val335=
NM_001354801.1:c.8+142G>C	NP_001341730.1:n.8+142G>C
NM_033507.2:c.1008G>C	NP_277042.1:p.Val336=
NM_033508.2:c.1002G>C	NP_277043.1:p.Val334=
NM_000162.5:c.1005G>C MANE Select	NP_000153.1:p.Val335=
NM_033507.3:c.1008G>C	NP_277042.1:p.Val336=
NM_033508.3:c.1002G>C	NP_277043.1:p.Val334=