Canonical Allele Identifier: CA157913871

Gene: GCK

Linked Data

• dbSNP Id: rs972271262
• gnomAD v2: 7-44185399-CCT-C
• gnomAD v3: 7-44145800-CCT-C
• gnomAD v4: 7-44145800-CCT-C
• MyVariant Identifiers: chr7:g.44185400_44185401del (hg19) ; chr7:g.44145801_44145802del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145804_44145805del , CM000669.2:g.44145804_44145805del	GRCh38
NC_000007.13:g.44185403_44185404del , CM000669.1:g.44185403_44185404del	GRCh37
NC_000007.12:g.44151928_44151929del	NCBI36
NG_008847.1:g.48622_48623del
NG_008847.2:g.57369_57370del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1018-72_*1018-71del	ENSP00000379142.4:n.*1018-72_*1018-71del
ENST00000616242.5:c.*140-72_*140-71del	ENSP00000482149.2:n.*140-72_*140-71del
ENST00000683378.1:n.246-72_246-71del
ENST00000336642.9:c.54-72_54-71del	ENSP00000338009.5:n.54-72_54-71del
ENST00000345378.7:c.1023-72_1023-71del	ENSP00000223366.2:n.1023-72_1023-71del
ENST00000403799.8:c.1020-72_1020-71del MANE Select	ENSP00000384247.3:n.1020-72_1020-71del
ENST00000671824.1:c.1083-72_1083-71del	ENSP00000500264.1:n.1083-72_1083-71del
ENST00000672743.1:n.32-72_32-71del
ENST00000673284.1:c.1020-72_1020-71del	ENSP00000499852.1:n.1020-72_1020-71del
ENST00000336642.8:c.72-72_72-71del	ENSP00000338009.4:n.72-72_72-71del
ENST00000345378.6:c.1023-72_1023-71del	ENSP00000223366.2:n.1023-72_1023-71del
ENST00000395796.7:c.1017-72_1017-71del	ENSP00000379142.3:n.1017-72_1017-71del
ENST00000403799.7:c.1020-72_1020-71del	ENSP00000384247.3:n.1020-72_1020-71del
ENST00000437084.1:c.969-72_969-71del	ENSP00000402840.1:n.969-72_969-71del
ENST00000459642.1:n.328_329del
ENST00000473353.1:n.318-72_318-71del
ENST00000616242.4:c.1017-72_1017-71del	ENSP00000482149.1:n.1017-72_1017-71del
NM_000162.3:c.1020-72_1020-71del	NP_000153.1:n.1020-72_1020-71del
NM_033507.1:c.1023-72_1023-71del	NP_277042.1:n.1023-72_1023-71del
NM_033508.1:c.1017-72_1017-71del	NP_277043.1:n.1017-72_1017-71del
NM_000162.4:c.1020-72_1020-71del	NP_000153.1:n.1020-72_1020-71del
NM_001354800.1:c.1020-72_1020-71del	NP_001341729.1:n.1020-72_1020-71del
NM_001354801.1:c.9-72_9-71del	NP_001341730.1:n.9-72_9-71del
NM_001354802.1:c.-121-72_-121-71del	NP_001341731.1:n.-121-72_-121-71del
NM_001354803.1:c.54-72_54-71del	NP_001341732.1:n.54-72_54-71del
NM_033507.2:c.1023-72_1023-71del	NP_277042.1:n.1023-72_1023-71del
NM_033508.2:c.1017-72_1017-71del	NP_277043.1:n.1017-72_1017-71del
XM_024446707.1:c.-121-72_-121-71del	XP_024302475.1:n.-121-72_-121-71del
NM_000162.5:c.1020-72_1020-71del MANE Select	NP_000153.1:n.1020-72_1020-71del
NM_033507.3:c.1023-72_1023-71del	NP_277042.1:n.1023-72_1023-71del
NM_033508.3:c.1017-72_1017-71del	NP_277043.1:n.1017-72_1017-71del
NM_001354803.2:c.54-72_54-71del	NP_001341732.1:n.54-72_54-71del