Canonical Allele Identifier: CA986871849

Gene: GCGR

Linked Data

• gnomAD v3: 17-81809694-CCTGCCTGCCTGTCTGCCTGTCTGTCTGCCTGTCTGT-C
• gnomAD v4: 17-81809694-CCTGCCTGCCTGTCTGCCTGTCTGTCTGCCTGTCTGT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809710_81809745del , CM000679.2:g.81809710_81809745del	GRCh38
NC_000017.10:g.79767586_79767621del , CM000679.1:g.79767586_79767621del	GRCh37
NG_016409.1:g.8537_8572del

Transcript Alleles

HGVS	Amino-acid change
ENST00000400723.8:c.61-72_61-37del MANE Select	ENSP00000383558.3:n.61-72_61-37del
ENST00000400723.7:c.61-72_61-37del	ENSP00000383558.3:n.61-72_61-37del
ENST00000570996.5:c.61-72_61-37del	ENSP00000460976.1:n.61-72_61-37del
ENST00000572185.1:n.356-72_356-37del
ENST00000573428.1:c.61-72_61-37del	ENSP00000458930.1:n.61-72_61-37del
NM_000160.4:c.61-72_61-37del	NP_000151.1:n.61-72_61-37del
XM_006722277.1:c.61-72_61-37del	XP_006722340.1:n.61-72_61-37del
XM_011523539.1:c.-166-72_-166-37del	XP_011521841.1:n.-166-72_-166-37del
XM_011523540.1:c.-456-72_-456-37del	XP_011521842.1:n.-456-72_-456-37del
XM_017024446.1:c.61-78_61-43del	XP_016879935.1:n.61-78_61-43del
XM_017024447.1:c.-450-78_-450-43del	XP_016879936.1:n.-450-78_-450-43del
NM_000160.5:c.61-72_61-37del MANE Select	NP_000151.1:n.61-72_61-37del