Canonical Allele Identifier: CA502298355

Gene: GCGR

Linked Data

• MyVariant Identifiers: chr17:g.79767756C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809880C>A , CM000679.2:g.81809880C>A	GRCh38
NC_000017.10:g.79767756C>A , CM000679.1:g.79767756C>A	GRCh37
NG_016409.1:g.8707C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.159C>A MANE Select	ENSP00000383558.3:p.Pro53=
ENST00000400723.7:c.159C>A	ENSP00000383558.3:p.Pro53=
ENST00000570996.5:c.159C>A	ENSP00000460976.1:p.Pro53=
ENST00000572185.1:n.454C>A
ENST00000573428.1:c.159C>A	ENSP00000458930.1:p.Pro53=
ENST00000574283.2:n.93C>A
NM_000160.4:c.159C>A	NP_000151.1:p.Pro53=
XM_006722277.1:c.159C>A	XP_006722340.1:p.Pro53=
XM_011523539.1:c.-68C>A	XP_011521841.1:n.-68C>A
XM_011523540.1:c.-358C>A	XP_011521842.1:n.-358C>A
XM_017024446.1:c.153C>A	XP_016879935.1:p.Pro51=
XM_017024447.1:c.-358C>A	XP_016879936.1:n.-358C>A
NM_000160.5:c.159C>A MANE Select	NP_000151.1:p.Pro53=