Canonical Allele Identifier: CA2078576228

Gene: SGCG

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23181058_23181059delinsCT , CM000675.2:g.23181058_23181059delinsCT	GRCh38
NC_000013.10:g.23755197_23755198delinsCT , CM000675.1:g.23755197_23755198delinsCT	GRCh37
NC_000013.9:g.22653197_22653198delinsCT	NCBI36
NG_008759.1:g.5138_5139delinsCT , LRG_207:g.5138_5139delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218867.4:c.-18_-17delinsCT MANE Select	ENSP00000218867.3:n.-18_-17delinsCT
ENST00000218867.3:c.-18_-17delinsCT	ENSP00000218867.3:n.-18_-17delinsCT
NM_000231.2:c.-18_-17delinsCT , LRG_207t1:c.-18_-17delinsCT	NP_000222.1:n.-18_-17delinsCT
XM_005266505.2:c.-169_-168delinsCT	XP_005266562.1:n.-169_-168delinsCT
XM_006719861.2:c.54+20412_54+20413delinsCT	XP_006719924.1:n.54+20412_54+20413delinsCT
XM_006719861.3:c.54+20412_54+20413delinsCT	XP_006719924.1:n.54+20412_54+20413delinsCT
XM_024449397.1:c.-152+75_-152+76delinsCT	XP_024305165.1:n.-152+75_-152+76delinsCT
NM_000231.3:c.-18_-17delinsCT MANE Select	NP_000222.2:n.-18_-17delinsCT
NM_001378244.1:c.54+20412_54+20413delinsCT	NP_001365173.1:n.54+20412_54+20413delinsCT
NM_001378245.1:c.-152+75_-152+76delinsCT	NP_001365174.1:n.-152+75_-152+76delinsCT
NM_001378246.1:c.-169_-168delinsCT	NP_001365175.1:n.-169_-168delinsCT