Canonical Allele Identifier: CA401490953

Gene: GCGR

Linked Data

• gnomAD v4: 17-81809800-C-A
• MyVariant Identifiers: chr17:g.79767676C>A (hg19) ; chr17:g.81809800C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809800C>A , CM000679.2:g.81809800C>A	GRCh38
NC_000017.10:g.79767676C>A , CM000679.1:g.79767676C>A	GRCh37
NG_016409.1:g.8627C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.79C>A MANE Select	ENSP00000383558.3:p.Gln27Lys
ENST00000400723.7:c.79C>A	ENSP00000383558.3:p.Gln27Lys
ENST00000570996.5:c.79C>A	ENSP00000460976.1:p.Gln27Lys
ENST00000572185.1:n.374C>A
ENST00000573428.1:c.79C>A	ENSP00000458930.1:p.Gln27Lys
ENST00000574283.2:n.13C>A
NM_000160.4:c.79C>A	NP_000151.1:p.Gln27Lys
XM_006722277.1:c.79C>A	XP_006722340.1:p.Gln27Lys
XM_011523539.1:c.-148C>A	XP_011521841.1:n.-148C>A
XM_011523540.1:c.-438C>A	XP_011521842.1:n.-438C>A
XM_017024446.1:c.73C>A	XP_016879935.1:p.Gln25Lys
XM_017024447.1:c.-438C>A	XP_016879936.1:n.-438C>A
NM_000160.5:c.79C>A MANE Select	NP_000151.1:p.Gln27Lys