Canonical Allele Identifier: CA401491582

Gene: GCGR

Linked Data

• MyVariant Identifiers: chr17:g.79767757A>T (hg19) ; chr17:g.81809881A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809881A>T , CM000679.2:g.81809881A>T	GRCh38
NC_000017.10:g.79767757A>T , CM000679.1:g.79767757A>T	GRCh37
NG_016409.1:g.8708A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.160A>T MANE Select	ENSP00000383558.3:p.Thr54Ser
ENST00000400723.7:c.160A>T	ENSP00000383558.3:p.Thr54Ser
ENST00000570996.5:c.160A>T	ENSP00000460976.1:p.Thr54Ser
ENST00000572185.1:n.455A>T
ENST00000573428.1:c.160A>T	ENSP00000458930.1:p.Thr54Ser
ENST00000574283.2:n.94A>T
NM_000160.4:c.160A>T	NP_000151.1:p.Thr54Ser
XM_006722277.1:c.160A>T	XP_006722340.1:p.Thr54Ser
XM_011523539.1:c.-67A>T	XP_011521841.1:n.-67A>T
XM_011523540.1:c.-357A>T	XP_011521842.1:n.-357A>T
XM_017024446.1:c.154A>T	XP_016879935.1:p.Thr52Ser
XM_017024447.1:c.-357A>T	XP_016879936.1:n.-357A>T
NM_000160.5:c.160A>T MANE Select	NP_000151.1:p.Thr54Ser