Canonical Allele Identifier: CA367401279

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44189404A>C (hg19) ; chr7:g.44149805A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44149805A>C , CM000669.2:g.44149805A>C	GRCh38
NC_000007.13:g.44189404A>C , CM000669.1:g.44189404A>C	GRCh37
NC_000007.12:g.44155929A>C	NCBI36
NG_008847.1:g.44619T>G
NG_008847.2:g.53366T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*632T>G	ENSP00000379142.4:n.*632T>G
ENST00000616242.5:c.634T>G	ENSP00000482149.2:p.Ser212Ala
ENST00000682635.1:n.1120T>G
ENST00000345378.7:c.637T>G	ENSP00000223366.2:p.Ser213Ala
ENST00000403799.8:c.634T>G MANE Select	ENSP00000384247.3:p.Ser212Ala
ENST00000671824.1:c.634T>G	ENSP00000500264.1:p.Ser212Ala
ENST00000673284.1:c.634T>G	ENSP00000499852.1:p.Ser212Ala
ENST00000345378.6:c.637T>G	ENSP00000223366.2:p.Ser213Ala
ENST00000395796.7:c.631T>G	ENSP00000379142.3:p.Ser211Ala
ENST00000403799.7:c.634T>G	ENSP00000384247.3:p.Ser212Ala
ENST00000437084.1:c.583T>G	ENSP00000402840.1:p.Ser195Ala
ENST00000616242.4:c.631T>G	ENSP00000482149.1:p.Ser211Ala
NM_000162.3:c.634T>G	NP_000153.1:p.Ser212Ala
NM_033507.1:c.637T>G	NP_277042.1:p.Ser213Ala
NM_033508.1:c.631T>G	NP_277043.1:p.Ser211Ala
NM_000162.4:c.634T>G	NP_000153.1:p.Ser212Ala
NM_001354800.1:c.634T>G	NP_001341729.1:p.Ser212Ala
NM_033507.2:c.637T>G	NP_277042.1:p.Ser213Ala
NM_033508.2:c.631T>G	NP_277043.1:p.Ser211Ala
NM_000162.5:c.634T>G MANE Select	NP_000153.1:p.Ser212Ala
NM_033507.3:c.637T>G	NP_277042.1:p.Ser213Ala
NM_033508.3:c.631T>G	NP_277043.1:p.Ser211Ala