Canonical Allele Identifier: CA367401248

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44189394T>G (hg19) ; chr7:g.44149795T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44149795T>G , CM000669.2:g.44149795T>G	GRCh38
NC_000007.13:g.44189394T>G , CM000669.1:g.44189394T>G	GRCh37
NC_000007.12:g.44155919T>G	NCBI36
NG_008847.1:g.44629A>C
NG_008847.2:g.53376A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*642A>C	ENSP00000379142.4:n.*642A>C
ENST00000616242.5:c.644A>C	ENSP00000482149.2:p.Tyr215Ser
ENST00000682635.1:n.1130A>C
ENST00000345378.7:c.647A>C	ENSP00000223366.2:p.Tyr216Ser
ENST00000403799.8:c.644A>C MANE Select	ENSP00000384247.3:p.Tyr215Ser
ENST00000671824.1:c.644A>C	ENSP00000500264.1:p.Tyr215Ser
ENST00000673284.1:c.644A>C	ENSP00000499852.1:p.Tyr215Ser
ENST00000345378.6:c.647A>C	ENSP00000223366.2:p.Tyr216Ser
ENST00000395796.7:c.641A>C	ENSP00000379142.3:p.Tyr214Ser
ENST00000403799.7:c.644A>C	ENSP00000384247.3:p.Tyr215Ser
ENST00000437084.1:c.593A>C	ENSP00000402840.1:p.Tyr198Ser
ENST00000616242.4:c.641A>C	ENSP00000482149.1:p.Tyr214Ser
NM_000162.3:c.644A>C	NP_000153.1:p.Tyr215Ser
NM_033507.1:c.647A>C	NP_277042.1:p.Tyr216Ser
NM_033508.1:c.641A>C	NP_277043.1:p.Tyr214Ser
NM_000162.4:c.644A>C	NP_000153.1:p.Tyr215Ser
NM_001354800.1:c.644A>C	NP_001341729.1:p.Tyr215Ser
NM_033507.2:c.647A>C	NP_277042.1:p.Tyr216Ser
NM_033508.2:c.641A>C	NP_277043.1:p.Tyr214Ser
NM_000162.5:c.644A>C MANE Select	NP_000153.1:p.Tyr215Ser
NM_033507.3:c.647A>C	NP_277042.1:p.Tyr216Ser
NM_033508.3:c.641A>C	NP_277043.1:p.Tyr214Ser