Canonical Allele Identifier: CA2587877048

Gene: C3

Linked Data

• gnomAD v4: 19-6709611-TCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709613_6709614del , CM000681.2:g.6709613_6709614del	GRCh38
NC_000019.9:g.6709624_6709625del , CM000681.1:g.6709624_6709625del	GRCh37
NC_000019.8:g.6660624_6660625del	NCBI36
NG_009557.1:g.16039_16040del , LRG_27:g.16039_16040del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1722+71_1722+72del	ENSP00000512083.1:n.1722+71_1722+72del
ENST00000695654.1:c.969+71_969+72del	ENSP00000512085.1:n.969+71_969+72del
ENST00000695655.1:c.786+71_786+72del	ENSP00000512086.1:n.786+71_786+72del
ENST00000695692.1:n.1209+71_1209+72del
ENST00000245907.11:c.1845+71_1845+72del MANE Select	ENSP00000245907.4:n.1845+71_1845+72del
ENST00000245907.10:c.1845+71_1845+72del	ENSP00000245907.4:n.1845+71_1845+72del
NM_000064.3:c.1845+71_1845+72del	NP_000055.2:n.1845+71_1845+72del
NM_000064.4:c.1845+71_1845+72del MANE Select	NP_000055.2:n.1845+71_1845+72del