Canonical Allele Identifier: CA2682574925

Gene: GCK

Linked Data

• gnomAD v4: 7-44189370-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44189370T>A , CM000669.2:g.44189370T>A	GRCh38
NC_000007.13:g.44228969T>A , CM000669.1:g.44228969T>A	GRCh37
NC_000007.12:g.44195494T>A	NCBI36
NG_008847.1:g.5054A>T
NG_008847.2:g.13801A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000616242.5:c.-417A>T	ENSP00000482149.2:n.-417A>T
ENST00000682635.1:n.70A>T
ENST00000403799.8:c.-417A>T MANE Select	ENSP00000384247.3:n.-417A>T
ENST00000671824.1:c.-417A>T	ENSP00000500264.1:n.-417A>T
ENST00000673284.1:c.-417A>T	ENSP00000499852.1:n.-417A>T
ENST00000403799.7:c.-417A>T	ENSP00000384247.3:n.-417A>T
ENST00000476008.1:n.480+8321A>T
NM_000162.3:c.-417A>T	NP_000153.1:n.-417A>T
NM_000162.4:c.-417A>T	NP_000153.1:n.-417A>T
NM_001354800.1:c.-417A>T	NP_001341729.1:n.-417A>T
NM_000162.5:c.-417A>T MANE Select	NP_000153.1:n.-417A>T