Canonical Allele Identifier: CA2587877607

Gene: C3

Linked Data

• gnomAD v4: 19-6709966-GGGGAGAGAGAGGGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709968_6709981del , CM000681.2:g.6709968_6709981del	GRCh38
NC_000019.9:g.6709979_6709992del , CM000681.1:g.6709979_6709992del	GRCh37
NC_000019.8:g.6660979_6660992del	NCBI36
NG_009557.1:g.15672_15685del , LRG_27:g.15672_15685del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-138_1564-125del	ENSP00000512083.1:n.1564-138_1564-125del
ENST00000695654.1:c.811-138_811-125del	ENSP00000512085.1:n.811-138_811-125del
ENST00000695655.1:c.592-102_592-89del	ENSP00000512086.1:n.592-102_592-89del
ENST00000695692.1:n.1051-138_1051-125del
ENST00000245907.11:c.1687-138_1687-125del MANE Select	ENSP00000245907.4:n.1687-138_1687-125del
ENST00000245907.10:c.1687-138_1687-125del	ENSP00000245907.4:n.1687-138_1687-125del
ENST00000600763.1:n.320-138_320-125del
NM_000064.3:c.1687-138_1687-125del	NP_000055.2:n.1687-138_1687-125del
NM_000064.4:c.1687-138_1687-125del MANE Select	NP_000055.2:n.1687-138_1687-125del