Canonical Allele Identifier: CA2540384037

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44189392G>C , CM000669.2:g.44189392G>C	GRCh38
NC_000007.13:g.44228991G>C , CM000669.1:g.44228991G>C	GRCh37
NC_000007.12:g.44195516G>C	NCBI36
NG_008847.1:g.5032C>G
NG_008847.2:g.13779C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000616242.5:c.-439C>G	ENSP00000482149.2:n.-439C>G
ENST00000682635.1:n.48C>G
ENST00000403799.8:c.-439C>G MANE Select	ENSP00000384247.3:n.-439C>G
ENST00000671824.1:c.-439C>G	ENSP00000500264.1:n.-439C>G
ENST00000673284.1:c.-439C>G	ENSP00000499852.1:n.-439C>G
ENST00000403799.7:c.-439C>G	ENSP00000384247.3:n.-439C>G
ENST00000476008.1:n.480+8299C>G
NM_000162.3:c.-439C>G	NP_000153.1:n.-439C>G
NM_000162.4:c.-439C>G	NP_000153.1:n.-439C>G
NM_001354800.1:c.-439C>G	NP_001341729.1:n.-439C>G
NM_000162.5:c.-439C>G MANE Select	NP_000153.1:n.-439C>G