Canonical Allele Identifier: CA454609131
Gene: GCK HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.44189429C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44149830C>G , CM000669.2:g.44149830C>G GRCh38
NC_000007.13:g.44189429C>G , CM000669.1:g.44189429C>G GRCh37
NC_000007.12:g.44155954C>G NCBI36
NG_008847.1:g.44594G>C
NG_008847.2:g.53341G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000395796.8:c.*607G>C ENSP00000379142.4:n.*607G>C
ENST00000616242.5:c.609G>C ENSP00000482149.2:p.Val203=
ENST00000682635.1:n.1095G>C
ENST00000345378.7:c.612G>C ENSP00000223366.2:p.Val204=
ENST00000403799.8:c.609G>C MANE Select ENSP00000384247.3:p.Val203=
ENST00000671824.1:c.609G>C ENSP00000500264.1:p.Val203=
ENST00000673284.1:c.609G>C ENSP00000499852.1:p.Val203=
ENST00000345378.6:c.612G>C ENSP00000223366.2:p.Val204=
ENST00000395796.7:c.606G>C ENSP00000379142.3:p.Val202=
ENST00000403799.7:c.609G>C ENSP00000384247.3:p.Val203=
ENST00000437084.1:c.558G>C ENSP00000402840.1:p.Val186=
ENST00000616242.4:n.606G>C ENSP00000482149.1:p.Val202=
NM_000162.3:c.609G>C NP_000153.1:p.Val203=
NM_033507.1:c.612G>C NP_277042.1:p.Val204=
NM_033508.1:c.606G>C NP_277043.1:p.Val202=
NM_000162.4:c.609G>C NP_000153.1:p.Val203=
NM_001354800.1:c.609G>C NP_001341729.1:p.Val203=
NM_033507.2:c.612G>C NP_277042.1:p.Val204=
NM_033508.2:c.606G>C NP_277043.1:p.Val202=
NM_000162.5:c.609G>C MANE Select NP_000153.1:p.Val203=
NM_033507.3:c.612G>C NP_277042.1:p.Val204=
NM_033508.3:c.606G>C NP_277043.1:p.Val202=