Canonical Allele Identifier: CA2320568641

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6714591_6714598delinsGCGGCTCA , CM000681.2:g.6714591_6714598delinsGCGGCTCA	GRCh38
NC_000019.9:g.6714602_6714609delinsGCGGCTCA , CM000681.1:g.6714602_6714609delinsGCGGCTCA	GRCh37
NC_000019.8:g.6665602_6665609delinsGCGGCTCA	NCBI36
NG_009557.1:g.11054_11061delinsTGAGCCGC , LRG_27:g.11054_11061delinsTGAGCCGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.382-152_382-145delinsTGAGCCGC	ENSP00000512083.1:n.382-152_382-145delinsTGAGCCGC
ENST00000245907.11:c.505-152_505-145delinsTGAGCCGC MANE Select	ENSP00000245907.4:n.505-152_505-145delinsTGAGCCGC
ENST00000245907.10:c.505-152_505-145delinsTGAGCCGC	ENSP00000245907.4:n.505-152_505-145delinsTGAGCCGC
NM_000064.3:c.505-152_505-145delinsTGAGCCGC	NP_000055.2:n.505-152_505-145delinsTGAGCCGC
NM_000064.4:c.505-152_505-145delinsTGAGCCGC MANE Select	NP_000055.2:n.505-152_505-145delinsTGAGCCGC