Canonical Allele Identifier: CA2622326041

Gene: SGCG

Linked Data

• gnomAD v4: 13-23203918-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23203920del , CM000675.2:g.23203920del	GRCh38
NC_000013.10:g.23778059del , CM000675.1:g.23778059del	GRCh37
NC_000013.9:g.22676059del	NCBI36
NG_008759.1:g.28000del , LRG_207:g.28000del

Transcript Alleles

HGVS	Amino-acid change
ENST00000218867.4:c.195+31del MANE Select	ENSP00000218867.3:n.195+31del
ENST00000218867.3:c.195+31del	ENSP00000218867.3:n.195+31del
NM_000231.2:c.195+31del , LRG_207t1:c.195+31del	NP_000222.1:n.195+31del
XM_005266505.2:c.195+31del	XP_005266562.1:n.195+31del
XM_006719861.2:c.249+31del	XP_006719924.1:n.249+31del
XM_006719861.3:c.249+31del	XP_006719924.1:n.249+31del
XM_024449397.1:c.195+31del	XP_024305165.1:n.195+31del
NM_000231.3:c.195+31del MANE Select	NP_000222.2:n.195+31del
NM_001378244.1:c.249+31del	NP_001365173.1:n.249+31del
NM_001378245.1:c.195+31del	NP_001365174.1:n.195+31del
NM_001378246.1:c.195+31del	NP_001365175.1:n.195+31del