Canonical Allele Identifier: CA367398442

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44185145T>C (hg19) ; chr7:g.44145546T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145546T>C , CM000669.2:g.44145546T>C	GRCh38
NC_000007.13:g.44185145T>C , CM000669.1:g.44185145T>C	GRCh37
NC_000007.12:g.44151670T>C	NCBI36
NG_008847.1:g.48878A>G
NG_008847.2:g.57625A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*1202A>G	ENSP00000379142.4:n.*1202A>G
ENST00000616242.5:c.*324A>G	ENSP00000482149.2:n.*324A>G
ENST00000683378.1:n.430A>G
ENST00000336642.9:c.238A>G	ENSP00000338009.5:p.Met80Val
ENST00000345378.7:c.1207A>G	ENSP00000223366.2:p.Met403Val
ENST00000403799.8:c.1204A>G MANE Select	ENSP00000384247.3:p.Met402Val
ENST00000671824.1:c.1267A>G	ENSP00000500264.1:p.Met423Val
ENST00000672743.1:n.216A>G
ENST00000673284.1:c.1204A>G	ENSP00000499852.1:p.Met402Val
ENST00000336642.8:c.256A>G	ENSP00000338009.4:p.Met86Val
ENST00000345378.6:c.1207A>G	ENSP00000223366.2:p.Met403Val
ENST00000395796.7:c.1201A>G	ENSP00000379142.3:p.Met401Val
ENST00000403799.7:c.1204A>G	ENSP00000384247.3:p.Met402Val
ENST00000437084.1:c.1153A>G	ENSP00000402840.1:p.Met385Val
ENST00000459642.1:n.584A>G
ENST00000616242.4:c.1201A>G	ENSP00000482149.1:p.Met401Val
NM_000162.3:c.1204A>G	NP_000153.1:p.Met402Val
NM_033507.1:c.1207A>G	NP_277042.1:p.Met403Val
NM_033508.1:c.1201A>G	NP_277043.1:p.Met401Val
NM_000162.4:c.1204A>G	NP_000153.1:p.Met402Val
NM_001354800.1:c.1204A>G	NP_001341729.1:p.Met402Val
NM_001354801.1:c.193A>G	NP_001341730.1:p.Met65Val
NM_001354802.1:c.64A>G	NP_001341731.1:p.Met22Val
NM_001354803.1:c.238A>G	NP_001341732.1:p.Met80Val
NM_033507.2:c.1207A>G	NP_277042.1:p.Met403Val
NM_033508.2:c.1201A>G	NP_277043.1:p.Met401Val
XM_024446707.1:c.64A>G	XP_024302475.1:p.Met22Val
NM_000162.5:c.1204A>G MANE Select	NP_000153.1:p.Met402Val
NM_033507.3:c.1207A>G	NP_277042.1:p.Met403Val
NM_033508.3:c.1201A>G	NP_277043.1:p.Met401Val
NM_001354803.2:c.238A>G	NP_001341732.1:p.Met80Val