Canonical Allele Identifier: CA454607861

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44186136G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44146537G>A , CM000669.2:g.44146537G>A	GRCh38
NC_000007.13:g.44186136G>A , CM000669.1:g.44186136G>A	GRCh37
NC_000007.12:g.44152661G>A	NCBI36
NG_008847.1:g.47887C>T
NG_008847.2:g.56634C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*943C>T	ENSP00000379142.4:n.*943C>T
ENST00000616242.5:c.*65C>T	ENSP00000482149.2:n.*65C>T
ENST00000683378.1:n.171C>T
ENST00000345378.7:c.948C>T	ENSP00000223366.2:p.Leu316=
ENST00000403799.8:c.945C>T MANE Select	ENSP00000384247.3:p.Leu315=
ENST00000671824.1:c.1008C>T	ENSP00000500264.1:p.Leu336=
ENST00000673284.1:c.945C>T	ENSP00000499852.1:p.Leu315=
ENST00000345378.6:c.948C>T	ENSP00000223366.2:p.Leu316=
ENST00000395796.7:c.942C>T	ENSP00000379142.3:p.Leu314=
ENST00000403799.7:c.945C>T	ENSP00000384247.3:p.Leu315=
ENST00000437084.1:c.894C>T	ENSP00000402840.1:p.Leu298=
ENST00000473353.1:n.243C>T
ENST00000616242.4:c.942C>T	ENSP00000482149.1:p.Leu314=
NM_000162.3:c.945C>T	NP_000153.1:p.Leu315=
NM_033507.1:c.948C>T	NP_277042.1:p.Leu316=
NM_033508.1:c.942C>T	NP_277043.1:p.Leu314=
NM_000162.4:c.945C>T	NP_000153.1:p.Leu315=
NM_001354800.1:c.945C>T	NP_001341729.1:p.Leu315=
NM_001354801.1:c.8+82C>T	NP_001341730.1:n.8+82C>T
NM_033507.2:c.948C>T	NP_277042.1:p.Leu316=
NM_033508.2:c.942C>T	NP_277043.1:p.Leu314=
NM_000162.5:c.945C>T MANE Select	NP_000153.1:p.Leu315=
NM_033507.3:c.948C>T	NP_277042.1:p.Leu316=
NM_033508.3:c.942C>T	NP_277043.1:p.Leu314=