Canonical Allele Identifier: CA573797950

Gene: GCK

Linked Data

• dbSNP Id: rs1418843448
• gnomAD v2: 7-44189785-GGCTCAGAGCAGCCCCATA-G
• gnomAD v3: 7-44150186-GGCTCAGAGCAGCCCCATA-G
• gnomAD v4: 7-44150186-GGCTCAGAGCAGCCCCATA-G
• MyVariant Identifiers: chr7:g.44189786_44189803del (hg19) ; chr7:g.44150187_44150204del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44150190_44150207del , CM000669.2:g.44150190_44150207del	GRCh38
NC_000007.13:g.44189789_44189806del , CM000669.1:g.44189789_44189806del	GRCh37
NC_000007.12:g.44156314_44156331del	NCBI36
NG_008847.1:g.44220_44237del
NG_008847.2:g.52967_52984del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*482-140_*482-123del	ENSP00000379142.4:n.*482-140_*482-123del
ENST00000616242.5:c.484-140_484-123del	ENSP00000482149.2:n.484-140_484-123del
ENST00000682635.1:n.970-140_970-123del
ENST00000345378.7:c.487-140_487-123del	ENSP00000223366.2:n.487-140_487-123del
ENST00000403799.8:c.484-140_484-123del MANE Select	ENSP00000384247.3:n.484-140_484-123del
ENST00000671824.1:c.484-140_484-123del	ENSP00000500264.1:n.484-140_484-123del
ENST00000673284.1:c.484-140_484-123del	ENSP00000499852.1:n.484-140_484-123del
ENST00000345378.6:c.487-140_487-123del	ENSP00000223366.2:n.487-140_487-123del
ENST00000395796.7:c.481-140_481-123del	ENSP00000379142.3:n.481-140_481-123del
ENST00000403799.7:c.484-140_484-123del	ENSP00000384247.3:n.484-140_484-123del
ENST00000437084.1:c.433-140_433-123del	ENSP00000402840.1:n.433-140_433-123del
ENST00000616242.4:c.481-140_481-123del	ENSP00000482149.1:n.481-140_481-123del
NM_000162.3:c.484-140_484-123del	NP_000153.1:n.484-140_484-123del
NM_033507.1:c.487-140_487-123del	NP_277042.1:n.487-140_487-123del
NM_033508.1:c.481-140_481-123del	NP_277043.1:n.481-140_481-123del
NM_000162.4:c.484-140_484-123del	NP_000153.1:n.484-140_484-123del
NM_001354800.1:c.484-140_484-123del	NP_001341729.1:n.484-140_484-123del
NM_033507.2:c.487-140_487-123del	NP_277042.1:n.487-140_487-123del
NM_033508.2:c.481-140_481-123del	NP_277043.1:n.481-140_481-123del
NM_000162.5:c.484-140_484-123del MANE Select	NP_000153.1:n.484-140_484-123del
NM_033507.3:c.487-140_487-123del	NP_277042.1:n.487-140_487-123del
NM_033508.3:c.481-140_481-123del	NP_277043.1:n.481-140_481-123del