Canonical Allele Identifier: CA2587878775

Gene: C3

Linked Data

• gnomAD v4: 19-6714552-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6714552_6714553insA , CM000681.2:g.6714552_6714553insA	GRCh38
NC_000019.9:g.6714563_6714564insA , CM000681.1:g.6714563_6714564insA	GRCh37
NC_000019.8:g.6665563_6665564insA	NCBI36
NG_009557.1:g.11099_11100insT , LRG_27:g.11099_11100insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.382-107_382-106insT	ENSP00000512083.1:n.382-107_382-106insT
ENST00000245907.11:c.505-107_505-106insT MANE Select	ENSP00000245907.4:n.505-107_505-106insT
ENST00000245907.10:c.505-107_505-106insT	ENSP00000245907.4:n.505-107_505-106insT
NM_000064.3:c.505-107_505-106insT	NP_000055.2:n.505-107_505-106insT
NM_000064.4:c.505-107_505-106insT MANE Select	NP_000055.2:n.505-107_505-106insT