Canonical Allele Identifier: CA367399889

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44186123C>A (hg19) ; chr7:g.44146524C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44146524C>A , CM000669.2:g.44146524C>A	GRCh38
NC_000007.13:g.44186123C>A , CM000669.1:g.44186123C>A	GRCh37
NC_000007.12:g.44152648C>A	NCBI36
NG_008847.1:g.47900G>T
NG_008847.2:g.56647G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*956G>T	ENSP00000379142.4:n.*956G>T
ENST00000616242.5:c.*78G>T	ENSP00000482149.2:n.*78G>T
ENST00000683378.1:n.184G>T
ENST00000345378.7:c.961G>T	ENSP00000223366.2:p.Ala321Ser
ENST00000403799.8:c.958G>T MANE Select	ENSP00000384247.3:p.Ala320Ser
ENST00000671824.1:c.1021G>T	ENSP00000500264.1:p.Ala341Ser
ENST00000673284.1:c.958G>T	ENSP00000499852.1:p.Ala320Ser
ENST00000345378.6:c.961G>T	ENSP00000223366.2:p.Ala321Ser
ENST00000395796.7:c.955G>T	ENSP00000379142.3:p.Ala319Ser
ENST00000403799.7:c.958G>T	ENSP00000384247.3:p.Ala320Ser
ENST00000437084.1:c.907G>T	ENSP00000402840.1:p.Ala303Ser
ENST00000473353.1:n.256G>T
ENST00000616242.4:c.955G>T	ENSP00000482149.1:p.Ala319Ser
NM_000162.3:c.958G>T	NP_000153.1:p.Ala320Ser
NM_033507.1:c.961G>T	NP_277042.1:p.Ala321Ser
NM_033508.1:c.955G>T	NP_277043.1:p.Ala319Ser
NM_000162.4:c.958G>T	NP_000153.1:p.Ala320Ser
NM_001354800.1:c.958G>T	NP_001341729.1:p.Ala320Ser
NM_001354801.1:c.8+95G>T	NP_001341730.1:n.8+95G>T
NM_033507.2:c.961G>T	NP_277042.1:p.Ala321Ser
NM_033508.2:c.955G>T	NP_277043.1:p.Ala319Ser
NM_000162.5:c.958G>T MANE Select	NP_000153.1:p.Ala320Ser
NM_033507.3:c.961G>T	NP_277042.1:p.Ala321Ser
NM_033508.3:c.955G>T	NP_277043.1:p.Ala319Ser