Canonical Allele Identifier: CA651535535

Gene: GCK

Linked Data

• COSMIC: COSN15041223

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44189379_44189380insC , CM000669.2:g.44189379_44189380insC	GRCh38
NC_000007.13:g.44228978_44228979insC , CM000669.1:g.44228978_44228979insC	GRCh37
NC_000007.12:g.44195503_44195504insC	NCBI36
NG_008847.1:g.5044_5045insG
NG_008847.2:g.13791_13792insG

Transcript Alleles

HGVS	Amino-acid change
ENST00000616242.5:c.-427_-426insG	ENSP00000482149.2:n.-427_-426insG
ENST00000682635.1:n.60_61insG
ENST00000403799.8:c.-427_-426insG MANE Select	ENSP00000384247.3:n.-427_-426insG
ENST00000671824.1:c.-427_-426insG	ENSP00000500264.1:n.-427_-426insG
ENST00000673284.1:c.-427_-426insG	ENSP00000499852.1:n.-427_-426insG
ENST00000403799.7:c.-427_-426insG	ENSP00000384247.3:n.-427_-426insG
ENST00000476008.1:n.480+8311_480+8312insG
NM_000162.3:c.-427_-426insG	NP_000153.1:n.-427_-426insG
NM_000162.4:c.-427_-426insG	NP_000153.1:n.-427_-426insG
NM_001354800.1:c.-427_-426insG	NP_001341729.1:n.-427_-426insG
NM_000162.5:c.-427_-426insG MANE Select	NP_000153.1:n.-427_-426insG