Canonical Allele Identifier: CA838795216

Gene: GCK

Linked Data

• dbSNP Id: rs1339865267
• gnomAD v4: 7-44189375-T-TCCTA
• MyVariant Identifiers: chr7:g.44228974_44228975insCCTA (hg19) ; chr7:g.44189375_44189376insCCTA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44189376_44189379dup , CM000669.2:g.44189376_44189379dup	GRCh38
NC_000007.13:g.44228975_44228978dup , CM000669.1:g.44228975_44228978dup	GRCh37
NC_000007.12:g.44195500_44195503dup	NCBI36
NG_008847.1:g.5045_5048dup
NG_008847.2:g.13792_13795dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000616242.5:c.-426_-423dup	ENSP00000482149.2:n.-426_-423dup
ENST00000682635.1:n.61_64dup
ENST00000403799.8:c.-426_-423dup MANE Select	ENSP00000384247.3:n.-426_-423dup
ENST00000671824.1:c.-426_-423dup	ENSP00000500264.1:n.-426_-423dup
ENST00000673284.1:c.-426_-423dup	ENSP00000499852.1:n.-426_-423dup
ENST00000403799.7:c.-426_-423dup	ENSP00000384247.3:n.-426_-423dup
ENST00000476008.1:n.480+8312_480+8315dup
NM_000162.3:c.-426_-423dup	NP_000153.1:n.-426_-423dup
NM_000162.4:c.-426_-423dup	NP_000153.1:n.-426_-423dup
NM_001354800.1:c.-426_-423dup	NP_001341729.1:n.-426_-423dup
NM_000162.5:c.-426_-423dup MANE Select	NP_000153.1:n.-426_-423dup