Canonical Allele Identifier: CA2578878028

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145805del , CM000669.2:g.44145805del	GRCh38
NC_000007.13:g.44185404del , CM000669.1:g.44185404del	GRCh37
NC_000007.12:g.44151929del	NCBI36
NG_008847.1:g.48619del
NG_008847.2:g.57366del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1018-75del	ENSP00000379142.4:n.*1018-75del
ENST00000616242.5:c.*140-75del	ENSP00000482149.2:n.*140-75del
ENST00000683378.1:n.246-75del
ENST00000336642.9:c.54-75del	ENSP00000338009.5:n.54-75del
ENST00000345378.7:c.1023-75del	ENSP00000223366.2:n.1023-75del
ENST00000403799.8:c.1020-75del MANE Select	ENSP00000384247.3:n.1020-75del
ENST00000671824.1:c.1083-75del	ENSP00000500264.1:n.1083-75del
ENST00000672743.1:n.32-75del
ENST00000673284.1:c.1020-75del	ENSP00000499852.1:n.1020-75del
ENST00000336642.8:c.72-75del	ENSP00000338009.4:n.72-75del
ENST00000345378.6:c.1023-75del	ENSP00000223366.2:n.1023-75del
ENST00000395796.7:c.1017-75del	ENSP00000379142.3:n.1017-75del
ENST00000403799.7:c.1020-75del	ENSP00000384247.3:n.1020-75del
ENST00000437084.1:c.969-75del	ENSP00000402840.1:n.969-75del
ENST00000459642.1:n.325del
ENST00000473353.1:n.318-75del
ENST00000616242.4:c.1017-75del	ENSP00000482149.1:n.1017-75del
NM_000162.3:c.1020-75del	NP_000153.1:n.1020-75del
NM_033507.1:c.1023-75del	NP_277042.1:n.1023-75del
NM_033508.1:c.1017-75del	NP_277043.1:n.1017-75del
NM_000162.4:c.1020-75del	NP_000153.1:n.1020-75del
NM_001354800.1:c.1020-75del	NP_001341729.1:n.1020-75del
NM_001354801.1:c.9-75del	NP_001341730.1:n.9-75del
NM_001354802.1:c.-121-75del	NP_001341731.1:n.-121-75del
NM_001354803.1:c.54-75del	NP_001341732.1:n.54-75del
NM_033507.2:c.1023-75del	NP_277042.1:n.1023-75del
NM_033508.2:c.1017-75del	NP_277043.1:n.1017-75del
XM_024446707.1:c.-121-75del	XP_024302475.1:n.-121-75del
NM_000162.5:c.1020-75del MANE Select	NP_000153.1:n.1020-75del
NM_033507.3:c.1023-75del	NP_277042.1:n.1023-75del
NM_033508.3:c.1017-75del	NP_277043.1:n.1017-75del
NM_001354803.2:c.54-75del	NP_001341732.1:n.54-75del