Canonical Allele Identifier: CA2682576410

Gene: GCK

Linked Data

• gnomAD v4: 7-44152491-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44152495del , CM000669.2:g.44152495del	GRCh38
NC_000007.13:g.44192094del , CM000669.1:g.44192094del	GRCh37
NC_000007.12:g.44158619del	NCBI36
NG_008847.1:g.41932del
NG_008847.2:g.50679del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*207-67del	ENSP00000379142.4:n.*207-67del
ENST00000616242.5:c.209-67del	ENSP00000482149.2:n.209-67del
ENST00000682635.1:n.695-67del
ENST00000345378.7:c.212-67del	ENSP00000223366.2:n.212-67del
ENST00000403799.8:c.209-67del MANE Select	ENSP00000384247.3:n.209-67del
ENST00000671824.1:c.209-67del	ENSP00000500264.1:n.209-67del
ENST00000673284.1:c.209-67del	ENSP00000499852.1:n.209-67del
ENST00000345378.6:c.212-67del	ENSP00000223366.2:n.212-67del
ENST00000395796.7:c.206-67del	ENSP00000379142.3:n.206-67del
ENST00000403799.7:c.209-67del	ENSP00000384247.3:n.209-67del
ENST00000437084.1:c.209-67del	ENSP00000402840.1:n.209-67del
ENST00000616242.4:c.206-67del	ENSP00000482149.1:n.206-67del
NM_000162.3:c.209-67del	NP_000153.1:n.209-67del
NM_033507.1:c.212-67del	NP_277042.1:n.212-67del
NM_033508.1:c.206-67del	NP_277043.1:n.206-67del
NM_000162.4:c.209-67del	NP_000153.1:n.209-67del
NM_001354800.1:c.209-67del	NP_001341729.1:n.209-67del
NM_033507.2:c.212-67del	NP_277042.1:n.212-67del
NM_033508.2:c.206-67del	NP_277043.1:n.206-67del
NM_000162.5:c.209-67del MANE Select	NP_000153.1:n.209-67del
NM_033507.3:c.212-67del	NP_277042.1:n.212-67del
NM_033508.3:c.206-67del	NP_277043.1:n.206-67del