Canonical Allele Identifier: CA2830550822

Gene: SGCG

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23250797_23250798insG , CM000675.2:g.23250797_23250798insG	GRCh38
NC_000013.10:g.23824936_23824937insG , CM000675.1:g.23824936_23824937insG	GRCh37
NC_000013.9:g.22722936_22722937insG	NCBI36
NG_008759.1:g.74877_74878insG , LRG_207:g.74877_74878insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218867.4:c.385+80_385+81insG MANE Select	ENSP00000218867.3:n.385+80_385+81insG
ENST00000218867.3:c.385+80_385+81insG	ENSP00000218867.3:n.385+80_385+81insG
NM_000231.2:c.385+80_385+81insG , LRG_207t1:c.385+80_385+81insG	NP_000222.1:n.385+80_385+81insG
XM_005266505.2:c.385+80_385+81insG	XP_005266562.1:n.385+80_385+81insG
XM_006719861.2:c.439+80_439+81insG	XP_006719924.1:n.439+80_439+81insG
XM_006719861.3:c.439+80_439+81insG	XP_006719924.1:n.439+80_439+81insG
XM_024449397.1:c.385+80_385+81insG	XP_024305165.1:n.385+80_385+81insG
NM_000231.3:c.385+80_385+81insG MANE Select	NP_000222.2:n.385+80_385+81insG
NM_001378244.1:c.439+80_439+81insG	NP_001365173.1:n.439+80_439+81insG
NM_001378245.1:c.385+80_385+81insG	NP_001365174.1:n.385+80_385+81insG
NM_001378246.1:c.385+80_385+81insG	NP_001365175.1:n.385+80_385+81insG