Canonical Allele Identifier: CA574226401

Gene: GCK

Linked Data

• dbSNP Id: rs1562715168
• gnomAD v2: 7-44187239-GC-G
• gnomAD v4: 7-44147640-GC-G
• MyVariant Identifiers: chr7:g.44187240del (hg19) ; chr7:g.44147641del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44147641del , CM000669.2:g.44147641del	GRCh38
NC_000007.13:g.44187240del , CM000669.1:g.44187240del	GRCh37
NC_000007.12:g.44153765del	NCBI36
NG_008847.1:g.46783del
NG_008847.2:g.55530del

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*861+9del	ENSP00000379142.4:n.*861+9del
ENST00000616242.5:c.853+19del	ENSP00000482149.2:n.853+19del
ENST00000345378.7:c.866+9del	ENSP00000223366.2:n.866+9del
ENST00000403799.8:c.863+9del MANE Select	ENSP00000384247.3:n.863+9del
ENST00000671824.1:c.853+19del	ENSP00000500264.1:n.853+19del
ENST00000673284.1:c.863+9del	ENSP00000499852.1:n.863+9del
ENST00000345378.6:c.866+9del	ENSP00000223366.2:n.866+9del
ENST00000395796.7:c.860+9del	ENSP00000379142.3:n.860+9del
ENST00000403799.7:c.863+9del	ENSP00000384247.3:n.863+9del
ENST00000437084.1:c.812+9del	ENSP00000402840.1:n.812+9del
ENST00000616242.4:c.860+9del	ENSP00000482149.1:n.860+9del
NM_000162.3:c.863+9del	NP_000153.1:n.863+9del
NM_033507.1:c.866+9del	NP_277042.1:n.866+9del
NM_033508.1:c.860+9del	NP_277043.1:n.860+9del
NM_000162.4:c.863+9del	NP_000153.1:n.863+9del
NM_001354800.1:c.863+9del	NP_001341729.1:n.863+9del
NM_033507.2:c.866+9del	NP_277042.1:n.866+9del
NM_033508.2:c.860+9del	NP_277043.1:n.860+9del
NM_000162.5:c.863+9del MANE Select	NP_000153.1:n.863+9del
NM_033507.3:c.866+9del	NP_277042.1:n.866+9del
NM_033508.3:c.860+9del	NP_277043.1:n.860+9del