Canonical Allele Identifier: CA2587877463

Gene: C3

Linked Data

• gnomAD v4: 19-6709639-CGTGCCTCCGCCTCTTCTCAGCAGCCTTGGGTCACTGG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709640_6709676del , CM000681.2:g.6709640_6709676del	GRCh38
NC_000019.9:g.6709651_6709687del , CM000681.1:g.6709651_6709687del	GRCh37
NC_000019.8:g.6660651_6660687del	NCBI36
NG_009557.1:g.15976_16012del , LRG_27:g.15976_16012del

Transcript Alleles

HGVS	Amino-acid change
ENST00000695652.1:c.1722+8_1722+44del	ENSP00000512083.1:n.1722+8_1722+44del
ENST00000695654.1:c.969+8_969+44del	ENSP00000512085.1:n.969+8_969+44del
ENST00000695655.1:c.786+8_786+44del	ENSP00000512086.1:n.786+8_786+44del
ENST00000695692.1:n.1209+8_1209+44del
ENST00000245907.11:c.1845+8_1845+44del MANE Select	ENSP00000245907.4:n.1845+8_1845+44del
ENST00000245907.10:c.1845+8_1845+44del	ENSP00000245907.4:n.1845+8_1845+44del
NM_000064.3:c.1845+8_1845+44del	NP_000055.2:n.1845+8_1845+44del
NM_000064.4:c.1845+8_1845+44del MANE Select	NP_000055.2:n.1845+8_1845+44del