Canonical Allele Identifier: CA367402756

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44191926T>G (hg19) ; chr7:g.44152327T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44152327T>G , CM000669.2:g.44152327T>G	GRCh38
NC_000007.13:g.44191926T>G , CM000669.1:g.44191926T>G	GRCh37
NC_000007.12:g.44158451T>G	NCBI36
NG_008847.1:g.42097A>C
NG_008847.2:g.50844A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*305A>C	ENSP00000379142.4:n.*305A>C
ENST00000616242.5:c.307A>C	ENSP00000482149.2:p.Thr103Pro
ENST00000682635.1:n.793A>C
ENST00000345378.7:c.310A>C	ENSP00000223366.2:p.Thr104Pro
ENST00000403799.8:c.307A>C MANE Select	ENSP00000384247.3:p.Thr103Pro
ENST00000671824.1:c.307A>C	ENSP00000500264.1:p.Thr103Pro
ENST00000673284.1:c.307A>C	ENSP00000499852.1:p.Thr103Pro
ENST00000345378.6:c.310A>C	ENSP00000223366.2:p.Thr104Pro
ENST00000395796.7:c.304A>C	ENSP00000379142.3:p.Thr102Pro
ENST00000403799.7:c.307A>C	ENSP00000384247.3:p.Thr103Pro
ENST00000437084.1:c.307A>C	ENSP00000402840.1:p.Thr103Pro
ENST00000616242.4:c.304A>C	ENSP00000482149.1:p.Thr102Pro
NM_000162.3:c.307A>C	NP_000153.1:p.Thr103Pro
NM_033507.1:c.310A>C	NP_277042.1:p.Thr104Pro
NM_033508.1:c.304A>C	NP_277043.1:p.Thr102Pro
NM_000162.4:c.307A>C	NP_000153.1:p.Thr103Pro
NM_001354800.1:c.307A>C	NP_001341729.1:p.Thr103Pro
NM_033507.2:c.310A>C	NP_277042.1:p.Thr104Pro
NM_033508.2:c.304A>C	NP_277043.1:p.Thr102Pro
NM_000162.5:c.307A>C MANE Select	NP_000153.1:p.Thr103Pro
NM_033507.3:c.310A>C	NP_277042.1:p.Thr104Pro
NM_033508.3:c.304A>C	NP_277043.1:p.Thr102Pro