Canonical Allele Identifier: CA986871552

Gene: GCGR

Linked Data

• dbSNP Id: rs2038049318
• gnomAD v3: 17-81809626-TCTGC-T
• gnomAD v4: 17-81809626-TCTGC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809634_81809637del , CM000679.2:g.81809634_81809637del	GRCh38
NC_000017.10:g.79767510_79767513del , CM000679.1:g.79767510_79767513del	GRCh37
NG_016409.1:g.8461_8464del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.61-148_61-145del MANE Select	ENSP00000383558.3:n.61-148_61-145del
ENST00000400723.7:c.61-148_61-145del	ENSP00000383558.3:n.61-148_61-145del
ENST00000570996.5:c.61-148_61-145del	ENSP00000460976.1:n.61-148_61-145del
ENST00000572185.1:n.356-148_356-145del
ENST00000573428.1:c.61-148_61-145del	ENSP00000458930.1:n.61-148_61-145del
NM_000160.4:c.61-148_61-145del	NP_000151.1:n.61-148_61-145del
XM_006722277.1:c.61-148_61-145del	XP_006722340.1:n.61-148_61-145del
XM_011523539.1:c.-166-148_-166-145del	XP_011521841.1:n.-166-148_-166-145del
XM_011523540.1:c.-456-148_-456-145del	XP_011521842.1:n.-456-148_-456-145del
XM_017024446.1:c.61-154_61-151del	XP_016879935.1:n.61-154_61-151del
XM_017024447.1:c.-450-154_-450-151del	XP_016879936.1:n.-450-154_-450-151del
NM_000160.5:c.61-148_61-145del MANE Select	NP_000151.1:n.61-148_61-145del