Canonical Allele Identifier: CA608609404

Gene: SGCG

Linked Data

• dbSNP Id: rs1196355071
• gnomAD v2: 13-23755243-A-AT
• gnomAD v3: 13-23181104-A-AT
• gnomAD v4: 13-23181104-A-AT
• MyVariant Identifiers: chr13:g.23755243_23755244insT (hg19) ; chr13:g.23181104_23181105insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23181105dup , CM000675.2:g.23181105dup	GRCh38
NC_000013.10:g.23755244dup , CM000675.1:g.23755244dup	GRCh37
NC_000013.9:g.22653244dup	NCBI36
NG_008759.1:g.5185dup , LRG_207:g.5185dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218867.4:c.-1+30dup MANE Select	ENSP00000218867.3:n.-1+30dup
ENST00000218867.3:c.-1+30dup	ENSP00000218867.3:n.-1+30dup
NM_000231.2:c.-1+30dup , LRG_207t1:c.-1+30dup	NP_000222.1:n.-1+30dup
XM_005266505.2:c.-152+30dup	XP_005266562.1:n.-152+30dup
XM_006719861.2:c.54+20459dup	XP_006719924.1:n.54+20459dup
XM_006719861.3:c.54+20459dup	XP_006719924.1:n.54+20459dup
XM_024449397.1:c.-152+122dup	XP_024305165.1:n.-152+122dup
NM_000231.3:c.-1+30dup MANE Select	NP_000222.2:n.-1+30dup
NM_001378244.1:c.54+20459dup	NP_001365173.1:n.54+20459dup
NM_001378245.1:c.-152+122dup	NP_001365174.1:n.-152+122dup
NM_001378246.1:c.-152+30dup	NP_001365175.1:n.-152+30dup