Canonical Allele Identifier: CA838783428

Gene: GCK

Linked Data

• dbSNP Id: rs1408020032
• MyVariant Identifiers: chr7:g.44192818_44192827del (hg19) ; chr7:g.44153219_44153228del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44153224_44153233del , CM000669.2:g.44153224_44153233del	GRCh38
NC_000007.13:g.44192823_44192832del , CM000669.1:g.44192823_44192832del	GRCh37
NC_000007.12:g.44159348_44159357del	NCBI36
NG_008847.1:g.41196_41205del
NG_008847.2:g.49943_49952del

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*206+73_*206+82del	ENSP00000379142.4:n.*206+73_*206+82del
ENST00000616242.5:c.208+73_208+82del	ENSP00000482149.2:n.208+73_208+82del
ENST00000682635.1:n.694+73_694+82del
ENST00000345378.7:c.211+73_211+82del	ENSP00000223366.2:n.211+73_211+82del
ENST00000403799.8:c.208+73_208+82del MANE Select	ENSP00000384247.3:n.208+73_208+82del
ENST00000671824.1:c.208+73_208+82del	ENSP00000500264.1:n.208+73_208+82del
ENST00000673284.1:c.208+73_208+82del	ENSP00000499852.1:n.208+73_208+82del
ENST00000345378.6:c.211+73_211+82del	ENSP00000223366.2:n.211+73_211+82del
ENST00000395796.7:c.205+73_205+82del	ENSP00000379142.3:n.205+73_205+82del
ENST00000403799.7:c.208+73_208+82del	ENSP00000384247.3:n.208+73_208+82del
ENST00000437084.1:c.208+73_208+82del	ENSP00000402840.1:n.208+73_208+82del
ENST00000616242.4:c.205+73_205+82del	ENSP00000482149.1:n.205+73_205+82del
NM_000162.3:c.208+73_208+82del	NP_000153.1:n.208+73_208+82del
NM_033507.1:c.211+73_211+82del	NP_277042.1:n.211+73_211+82del
NM_033508.1:c.205+73_205+82del	NP_277043.1:n.205+73_205+82del
NM_000162.4:c.208+73_208+82del	NP_000153.1:n.208+73_208+82del
NM_001354800.1:c.208+73_208+82del	NP_001341729.1:n.208+73_208+82del
NM_033507.2:c.211+73_211+82del	NP_277042.1:n.211+73_211+82del
NM_033508.2:c.205+73_205+82del	NP_277043.1:n.205+73_205+82del
NM_000162.5:c.208+73_208+82del MANE Select	NP_000153.1:n.208+73_208+82del
NM_033507.3:c.211+73_211+82del	NP_277042.1:n.211+73_211+82del
NM_033508.3:c.205+73_205+82del	NP_277043.1:n.205+73_205+82del