Canonical Allele Identifier: CA2682574994

Gene: GCK

Linked Data

• gnomAD v4: 7-44189391-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44189395del , CM000669.2:g.44189395del	GRCh38
NC_000007.13:g.44228994del , CM000669.1:g.44228994del	GRCh37
NC_000007.12:g.44195519del	NCBI36
NG_008847.1:g.5032del
NG_008847.2:g.13779del

Transcript Alleles

HGVS	Amino-acid change
ENST00000616242.5:c.-439del	ENSP00000482149.2:n.-439del
ENST00000682635.1:n.48del
ENST00000403799.8:c.-439del MANE Select	ENSP00000384247.3:n.-439del
ENST00000671824.1:c.-439del	ENSP00000500264.1:n.-439del
ENST00000673284.1:c.-439del	ENSP00000499852.1:n.-439del
ENST00000403799.7:c.-439del	ENSP00000384247.3:n.-439del
ENST00000476008.1:n.480+8299del
NM_000162.3:c.-439del	NP_000153.1:n.-439del
NM_000162.4:c.-439del	NP_000153.1:n.-439del
NM_001354800.1:c.-439del	NP_001341729.1:n.-439del
NM_000162.5:c.-439del MANE Select	NP_000153.1:n.-439del