Canonical Allele Identifier: CA2682584876

Gene: GCK

Linked Data

• gnomAD v4: 7-44146271-TCGGGCCCCGCCCACTCCCCCGCCCCCTGTGCCCCGCCCCGGGCCCCGCCCACGCCCGGAATCCCGCCCCAGGCCCTAGTTTCCCATCCCTGCGCCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44146278_44146373del , CM000669.2:g.44146278_44146373del	GRCh38
NC_000007.13:g.44185877_44185972del , CM000669.1:g.44185877_44185972del	GRCh37
NC_000007.12:g.44152402_44152497del	NCBI36
NG_008847.1:g.48057_48152del
NG_008847.2:g.56804_56899del

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*1017+96_*1017+191del	ENSP00000379142.4:n.*1017+96_*1017+191del...
ENST00000616242.5:c.*139+96_*139+191del	ENSP00000482149.2:n.*139+96_*139+191del
ENST00000683378.1:n.245+96_245+191del
ENST00000345378.7:c.1022+96_1022+191del	ENSP00000223366.2:n.1022+96_1022+191del
ENST00000403799.8:c.1019+96_1019+191del MANE Select	ENSP00000384247.3:n.1019+96_1019+191del
ENST00000671824.1:c.1082+96_1082+191del	ENSP00000500264.1:n.1082+96_1082+191del
ENST00000673284.1:c.1019+96_1019+191del	ENSP00000499852.1:n.1019+96_1019+191del
ENST00000345378.6:c.1022+96_1022+191del	ENSP00000223366.2:n.1022+96_1022+191del
ENST00000395796.7:c.1016+96_1016+191del	ENSP00000379142.3:n.1016+96_1016+191del
ENST00000403799.7:c.1019+96_1019+191del	ENSP00000384247.3:n.1019+96_1019+191del
ENST00000437084.1:c.968+96_968+191del	ENSP00000402840.1:n.968+96_968+191del
ENST00000473353.1:n.317+96_317+191del
ENST00000616242.4:c.1016+96_1016+191del	ENSP00000482149.1:n.1016+96_1016+191del
NM_000162.3:c.1019+96_1019+191del	NP_000153.1:n.1019+96_1019+191del
NM_033507.1:c.1022+96_1022+191del	NP_277042.1:n.1022+96_1022+191del
NM_033508.1:c.1016+96_1016+191del	NP_277043.1:n.1016+96_1016+191del
NM_000162.4:c.1019+96_1019+191del	NP_000153.1:n.1019+96_1019+191del
NM_001354800.1:c.1019+96_1019+191del	NP_001341729.1:n.1019+96_1019+191del
NM_001354801.1:c.8+252_8+347del	NP_001341730.1:n.8+252_8+347del
NM_033507.2:c.1022+96_1022+191del	NP_277042.1:n.1022+96_1022+191del
NM_033508.2:c.1016+96_1016+191del	NP_277043.1:n.1016+96_1016+191del
NM_000162.5:c.1019+96_1019+191del MANE Select	NP_000153.1:n.1019+96_1019+191del
NM_033507.3:c.1022+96_1022+191del	NP_277042.1:n.1022+96_1022+191del
NM_033508.3:c.1016+96_1016+191del	NP_277043.1:n.1016+96_1016+191del