Canonical Allele Identifier: CA482903244

Gene: SGCG

Linked Data

• MyVariant Identifiers: chr13:g.23778029_23778030insT (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23203891dup , CM000675.2:g.23203891dup	GRCh38
NC_000013.10:g.23778030dup , CM000675.1:g.23778030dup	GRCh37
NC_000013.9:g.22676030dup	NCBI36
NG_008759.1:g.27971dup , LRG_207:g.27971dup

Transcript Alleles

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