Canonical Allele Identifier: CA2640508802

Gene: GCGR

Linked Data

• gnomAD v4: 17-81809705-GTCTGCCTGTCTGTCTGCCTGTCTGTCTGCCTGCCTGTC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809707_81809744del , CM000679.2:g.81809707_81809744del	GRCh38
NC_000017.10:g.79767583_79767620del , CM000679.1:g.79767583_79767620del	GRCh37
NG_016409.1:g.8534_8571del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.61-75_61-38del MANE Select	ENSP00000383558.3:n.61-75_61-38del
ENST00000400723.7:c.61-75_61-38del	ENSP00000383558.3:n.61-75_61-38del
ENST00000570996.5:c.61-75_61-38del	ENSP00000460976.1:n.61-75_61-38del
ENST00000572185.1:n.356-75_356-38del
ENST00000573428.1:c.61-75_61-38del	ENSP00000458930.1:n.61-75_61-38del
NM_000160.4:c.61-75_61-38del	NP_000151.1:n.61-75_61-38del
XM_006722277.1:c.61-75_61-38del	XP_006722340.1:n.61-75_61-38del
XM_011523539.1:c.-166-75_-166-38del	XP_011521841.1:n.-166-75_-166-38del
XM_011523540.1:c.-456-75_-456-38del	XP_011521842.1:n.-456-75_-456-38del
XM_017024446.1:c.61-81_61-44del	XP_016879935.1:n.61-81_61-44del
XM_017024447.1:c.-450-81_-450-44del	XP_016879936.1:n.-450-81_-450-44del
NM_000160.5:c.61-75_61-38del MANE Select	NP_000151.1:n.61-75_61-38del