Canonical Allele Identifier: CA2640508729

Gene: GCGR

Linked Data

• gnomAD v4: 17-81809653-GCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809654_81809655del , CM000679.2:g.81809654_81809655del	GRCh38
NC_000017.10:g.79767530_79767531del , CM000679.1:g.79767530_79767531del	GRCh37
NG_016409.1:g.8481_8482del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.61-128_61-127del MANE Select	ENSP00000383558.3:n.61-128_61-127del
ENST00000400723.7:c.61-128_61-127del	ENSP00000383558.3:n.61-128_61-127del
ENST00000570996.5:c.61-128_61-127del	ENSP00000460976.1:n.61-128_61-127del
ENST00000572185.1:n.356-128_356-127del
ENST00000573428.1:c.61-128_61-127del	ENSP00000458930.1:n.61-128_61-127del
NM_000160.4:c.61-128_61-127del	NP_000151.1:n.61-128_61-127del
XM_006722277.1:c.61-128_61-127del	XP_006722340.1:n.61-128_61-127del
XM_011523539.1:c.-166-128_-166-127del	XP_011521841.1:n.-166-128_-166-127del
XM_011523540.1:c.-456-128_-456-127del	XP_011521842.1:n.-456-128_-456-127del
XM_017024446.1:c.61-134_61-133del	XP_016879935.1:n.61-134_61-133del
XM_017024447.1:c.-450-134_-450-133del	XP_016879936.1:n.-450-134_-450-133del
NM_000160.5:c.61-128_61-127del MANE Select	NP_000151.1:n.61-128_61-127del