Canonical Allele Identifier: CA954027282

Gene: SGCG

Linked Data

• gnomAD v3: 13-23181040-AGT-A
• gnomAD v4: 13-23181040-AGT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23181041_23181042del , CM000675.2:g.23181041_23181042del	GRCh38
NC_000013.10:g.23755180_23755181del , CM000675.1:g.23755180_23755181del	GRCh37
NC_000013.9:g.22653180_22653181del	NCBI36
NG_008759.1:g.5121_5122del , LRG_207:g.5121_5122del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218867.4:c.-35_-34del MANE Select	ENSP00000218867.3:n.-35_-34del
ENST00000218867.3:c.-35_-34del	ENSP00000218867.3:n.-35_-34del
NM_000231.2:c.-35_-34del , LRG_207t1:c.-35_-34del	NP_000222.1:n.-35_-34del
XM_005266505.2:c.-186_-185del	XP_005266562.1:n.-186_-185del
XM_006719861.2:c.54+20395_54+20396del	XP_006719924.1:n.54+20395_54+20396del
XM_006719861.3:c.54+20395_54+20396del	XP_006719924.1:n.54+20395_54+20396del
XM_024449397.1:c.-152+58_-152+59del	XP_024305165.1:n.-152+58_-152+59del
NM_000231.3:c.-35_-34del MANE Select	NP_000222.2:n.-35_-34del
NM_001378244.1:c.54+20395_54+20396del	NP_001365173.1:n.54+20395_54+20396del
NM_001378245.1:c.-152+58_-152+59del	NP_001365174.1:n.-152+58_-152+59del
NM_001378246.1:c.-186_-185del	NP_001365175.1:n.-186_-185del