Canonical Allele Identifier: CA2587872249

Gene: C3

Linked Data

• gnomAD v4: 19-6682267-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6682271del , CM000681.2:g.6682271del	GRCh38
NC_000019.9:g.6682282del , CM000681.1:g.6682282del	GRCh37
NC_000019.8:g.6633282del	NCBI36
NG_009557.1:g.43384del , LRG_27:g.43384del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2521-39del
ENST00000695653.1:c.2082-39del	ENSP00000512084.1:n.2082-39del
ENST00000695654.1:c.3198-39del	ENSP00000512085.1:n.3198-39del
ENST00000695689.1:c.144-39del	ENSP00000512101.1:n.144-39del
ENST00000695690.1:n.364-39del
ENST00000695691.1:n.364-39del
ENST00000245907.11:c.4173-39del MANE Select	ENSP00000245907.4:n.4173-39del
ENST00000245907.10:c.4173-39del	ENSP00000245907.4:n.4173-39del
ENST00000596548.1:c.294-39del	ENSP00000469744.1:n.294-39del
ENST00000599899.5:n.1093del
ENST00000601008.1:c.242-4310del	ENSP00000471384.1:n.242-4310del
NM_000064.3:c.4173-39del	NP_000055.2:n.4173-39del
NM_000064.4:c.4173-39del MANE Select	NP_000055.2:n.4173-39del