Canonical Allele Identifier: CA2695203065

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44146547dup , CM000669.2:g.44146547dup	GRCh38
NC_000007.13:g.44186146dup , CM000669.1:g.44186146dup	GRCh37
NC_000007.12:g.44152671dup	NCBI36
NG_008847.1:g.47880dup
NG_008847.2:g.56627dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*936dup	ENSP00000379142.4:n.*936dup
ENST00000616242.5:c.*58dup	ENSP00000482149.2:n.*58dup
ENST00000683378.1:n.164dup
ENST00000345378.7:c.941dup	ENSP00000223366.2:p.Asn314LysfsTer?
ENST00000403799.8:c.938dup MANE Select	ENSP00000384247.3:p.Asn313LysfsTer?
ENST00000671824.1:c.1001dup	ENSP00000500264.1:p.Asn334LysfsTer?
ENST00000673284.1:c.938dup	ENSP00000499852.1:p.Asn313LysfsTer?
ENST00000345378.6:c.941dup	ENSP00000223366.2:p.Asn314LysfsTer?
ENST00000395796.7:c.935dup	ENSP00000379142.3:p.Asn312LysfsTer?
ENST00000403799.7:c.938dup	ENSP00000384247.3:p.Asn313LysfsTer?
ENST00000437084.1:c.887dup	ENSP00000402840.1:p.Asn296LysfsTer?
ENST00000473353.1:n.236dup
ENST00000616242.4:c.935dup	ENSP00000482149.1:p.Asn312LysfsTer?
NM_000162.3:c.938dup	NP_000153.1:p.Asn313LysfsTer?
NM_033507.1:c.941dup	NP_277042.1:p.Asn314LysfsTer?
NM_033508.1:c.935dup	NP_277043.1:p.Asn312LysfsTer?
NM_000162.4:c.938dup	NP_000153.1:p.Asn313LysfsTer?
NM_001354800.1:c.938dup	NP_001341729.1:p.Asn313LysfsTer?
NM_001354801.1:c.8+75dup	NP_001341730.1:n.8+75dup
NM_033507.2:c.941dup	NP_277042.1:p.Asn314LysfsTer?
NM_033508.2:c.935dup	NP_277043.1:p.Asn312LysfsTer?
NM_000162.5:c.938dup MANE Select	NP_000153.1:p.Asn313LysfsTer?
NM_033507.3:c.941dup	NP_277042.1:p.Asn314LysfsTer?
NM_033508.3:c.935dup	NP_277043.1:p.Asn312LysfsTer?