Canonical Allele Identifier: CA367399762

Gene: GCK

Linked Data

• gnomAD v4: 7-44146485-G-T
• MyVariant Identifiers: chr7:g.44186084G>T (hg19) ; chr7:g.44146485G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44146485G>T , CM000669.2:g.44146485G>T	GRCh38
NC_000007.13:g.44186084G>T , CM000669.1:g.44186084G>T	GRCh37
NC_000007.12:g.44152609G>T	NCBI36
NG_008847.1:g.47939C>A
NG_008847.2:g.56686C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*995C>A	ENSP00000379142.4:n.*995C>A
ENST00000616242.5:c.*117C>A	ENSP00000482149.2:n.*117C>A
ENST00000683378.1:n.223C>A
ENST00000345378.7:c.1000C>A	ENSP00000223366.2:p.Arg334Ser
ENST00000403799.8:c.997C>A MANE Select	ENSP00000384247.3:p.Arg333Ser
ENST00000671824.1:c.1060C>A	ENSP00000500264.1:p.Arg354Ser
ENST00000673284.1:c.997C>A	ENSP00000499852.1:p.Arg333Ser
ENST00000345378.6:c.1000C>A	ENSP00000223366.2:p.Arg334Ser
ENST00000395796.7:c.994C>A	ENSP00000379142.3:p.Arg332Ser
ENST00000403799.7:c.997C>A	ENSP00000384247.3:p.Arg333Ser
ENST00000437084.1:c.946C>A	ENSP00000402840.1:p.Arg316Ser
ENST00000473353.1:n.295C>A
ENST00000616242.4:c.994C>A	ENSP00000482149.1:p.Arg332Ser
NM_000162.3:c.997C>A	NP_000153.1:p.Arg333Ser
NM_033507.1:c.1000C>A	NP_277042.1:p.Arg334Ser
NM_033508.1:c.994C>A	NP_277043.1:p.Arg332Ser
NM_000162.4:c.997C>A	NP_000153.1:p.Arg333Ser
NM_001354800.1:c.997C>A	NP_001341729.1:p.Arg333Ser
NM_001354801.1:c.8+134C>A	NP_001341730.1:n.8+134C>A
NM_033507.2:c.1000C>A	NP_277042.1:p.Arg334Ser
NM_033508.2:c.994C>A	NP_277043.1:p.Arg332Ser
NM_000162.5:c.997C>A MANE Select	NP_000153.1:p.Arg333Ser
NM_033507.3:c.1000C>A	NP_277042.1:p.Arg334Ser
NM_033508.3:c.994C>A	NP_277043.1:p.Arg332Ser