Canonical Allele Identifier: CA993073547

Gene: C3

Linked Data

• gnomAD v3: 19-6710014-AGG-A
• gnomAD v4: 19-6710014-AGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710016_6710017del , CM000681.2:g.6710016_6710017del	GRCh38
NC_000019.9:g.6710027_6710028del , CM000681.1:g.6710027_6710028del	GRCh37
NC_000019.8:g.6661027_6661028del	NCBI36
NG_009557.1:g.15636_15637del , LRG_27:g.15636_15637del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-174_1564-173del	ENSP00000512083.1:n.1564-174_1564-173del
ENST00000695654.1:c.811-174_811-173del	ENSP00000512085.1:n.811-174_811-173del
ENST00000695655.1:c.592-138_592-137del	ENSP00000512086.1:n.592-138_592-137del
ENST00000695692.1:n.1051-174_1051-173del
ENST00000245907.11:c.1687-174_1687-173del MANE Select	ENSP00000245907.4:n.1687-174_1687-173del
ENST00000245907.10:c.1687-174_1687-173del	ENSP00000245907.4:n.1687-174_1687-173del
ENST00000600763.1:n.320-174_320-173del
NM_000064.3:c.1687-174_1687-173del	NP_000055.2:n.1687-174_1687-173del
NM_000064.4:c.1687-174_1687-173del MANE Select	NP_000055.2:n.1687-174_1687-173del