Canonical Allele Identifier: CA4239361

Gene: GCK

Linked Data

• dbSNP Id: rs772098899
• ExAC: 7:44184694 GTGGGGCTGTGGCATCCTCCCTGCGCT / G
• gnomAD v2: 7-44184694-GTGGGGCTGTGGCATCCTCCCTGCGCT-G
• gnomAD v3: 7-44145095-GTGGGGCTGTGGCATCCTCCCTGCGCT-G
• gnomAD v4: 7-44145095-GTGGGGCTGTGGCATCCTCCCTGCGCT-G
• MyVariant Identifiers: chr7:g.44184695_44184720del (hg19) ; chr7:g.44145096_44145121del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145098_44145123del , CM000669.2:g.44145098_44145123del	GRCh38
NC_000007.13:g.44184697_44184722del , CM000669.1:g.44184697_44184722del	GRCh37
NC_000007.12:g.44151222_44151247del	NCBI36
NG_008847.1:g.49303_49328del
NG_008847.2:g.58050_58075del

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*1411_*1436del	ENSP00000379142.4:n.*1411_*1436del
ENST00000616242.5:c.*533_*558del	ENSP00000482149.2:n.*533_*558del
ENST00000683378.1:n.639_664del
ENST00000336642.9:c.*15_*40del	ENSP00000338009.5:n.*15_*40del
ENST00000345378.7:c.*15_*40del	ENSP00000223366.2:n.*15_*40del
ENST00000403799.8:c.*15_*40del MANE Select	ENSP00000384247.3:n.*15_*40del
ENST00000671824.1:c.*15_*40del	ENSP00000500264.1:n.*15_*40del
ENST00000672743.1:n.381+44_381+69del
ENST00000673284.1:c.1369+44_1369+69del	ENSP00000499852.1:n.1369+44_1369+69del
ENST00000336642.8:c.465_490del	ENSP00000338009.4:n.465_490del
ENST00000345378.6:c.*15_*40del	ENSP00000223366.2:n.*15_*40del
ENST00000395796.7:c.*15_*40del	ENSP00000379142.3:n.*15_*40del
ENST00000403799.7:c.*15_*40del	ENSP00000384247.3:n.*15_*40del
ENST00000459642.1:n.793_818del
ENST00000616242.4:c.1410_1435del	ENSP00000482149.1:n.1410_1435del
NM_000162.3:c.*15_*40del	NP_000153.1:n.*15_*40del
NM_033507.1:c.*15_*40del	NP_277042.1:n.*15_*40del
NM_033508.1:c.*15_*40del	NP_277043.1:n.*15_*40del
NM_000162.4:c.*15_*40del	NP_000153.1:n.*15_*40del
NM_001354800.1:c.1369+44_1369+69del	NP_001341729.1:n.1369+44_1369+69del
NM_001354801.1:c.*15_*40del	NP_001341730.1:n.*15_*40del
NM_001354802.1:c.229+44_229+69del	NP_001341731.1:n.229+44_229+69del
NM_001354803.1:c.*15_*40del	NP_001341732.1:n.*15_*40del
NM_033507.2:c.*15_*40del	NP_277042.1:n.*15_*40del
NM_033508.2:c.*15_*40del	NP_277043.1:n.*15_*40del
XM_024446707.1:c.*15_*40del	XP_024302475.1:n.*15_*40del
NM_000162.5:c.*15_*40del MANE Select	NP_000153.1:n.*15_*40del
NM_033507.3:c.*15_*40del	NP_277042.1:n.*15_*40del
NM_033508.3:c.*15_*40del	NP_277043.1:n.*15_*40del
NM_001354803.2:c.*15_*40del	NP_001341732.1:n.*15_*40del