Canonical Allele Identifier: CA2695203092

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44147732del , CM000669.2:g.44147732del	GRCh38
NC_000007.13:g.44187331del , CM000669.1:g.44187331del	GRCh37
NC_000007.12:g.44153856del	NCBI36
NG_008847.1:g.46695del
NG_008847.2:g.55442del

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*782del	ENSP00000379142.4:n.*782del
ENST00000616242.5:c.784del	ENSP00000482149.2:p.Asp262ThrfsTer25
ENST00000345378.7:c.787del	ENSP00000223366.2:p.Asp263ThrfsTer?
ENST00000403799.8:c.784del MANE Select	ENSP00000384247.3:p.Asp262ThrfsTer?
ENST00000671824.1:c.784del	ENSP00000500264.1:p.Asp262ThrfsTer?
ENST00000673284.1:c.784del	ENSP00000499852.1:p.Asp262ThrfsTer?
ENST00000345378.6:c.787del	ENSP00000223366.2:p.Asp263ThrfsTer?
ENST00000395796.7:c.781del	ENSP00000379142.3:p.Asp261ThrfsTer?
ENST00000403799.7:c.784del	ENSP00000384247.3:p.Asp262ThrfsTer?
ENST00000437084.1:c.733del	ENSP00000402840.1:p.Asp245ThrfsTer?
ENST00000616242.4:c.781del	ENSP00000482149.1:p.Asp261ThrfsTer?
NM_000162.3:c.784del	NP_000153.1:p.Asp262ThrfsTer?
NM_033507.1:c.787del	NP_277042.1:p.Asp263ThrfsTer?
NM_033508.1:c.781del	NP_277043.1:p.Asp261ThrfsTer?
XR_927223.1:n.66del
NM_000162.4:c.784del	NP_000153.1:p.Asp262ThrfsTer?
NM_001354800.1:c.784del	NP_001341729.1:p.Asp262ThrfsTer?
NM_033507.2:c.787del	NP_277042.1:p.Asp263ThrfsTer?
NM_033508.2:c.781del	NP_277043.1:p.Asp261ThrfsTer?
XR_927223.2:n.66del
NM_000162.5:c.784del MANE Select	NP_000153.1:p.Asp262ThrfsTer?
NM_033507.3:c.787del	NP_277042.1:p.Asp263ThrfsTer?
NM_033508.3:c.781del	NP_277043.1:p.Asp261ThrfsTer?