Canonical Allele Identifier: CA2576591726

Gene: C3

Linked Data

• gnomAD v4: 19-6679505-AGATGT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679513_6679517del , CM000681.2:g.6679513_6679517del	GRCh38
NC_000019.9:g.6679524_6679528del , CM000681.1:g.6679524_6679528del	GRCh37
NC_000019.8:g.6630524_6630528del	NCBI36
NG_009557.1:g.46142_46146del , LRG_27:g.46142_46146del

Transcript Alleles

HGVS	Amino-acid change
ENST00000695651.1:n.2805-14_2805-10del
ENST00000695653.1:c.2366-14_2366-10del	ENSP00000512084.1:n.2366-14_2366-10del
ENST00000695654.1:c.3482-14_3482-10del	ENSP00000512085.1:n.3482-14_3482-10del
ENST00000695689.1:c.428-14_428-10del	ENSP00000512101.1:n.428-14_428-10del
ENST00000695690.1:n.1522-14_1522-10del
ENST00000695691.1:n.1318-14_1318-10del
ENST00000245907.11:c.4457-14_4457-10del MANE Select	ENSP00000245907.4:n.4457-14_4457-10del
ENST00000245907.10:c.4457-14_4457-10del	ENSP00000245907.4:n.4457-14_4457-10del
ENST00000599668.1:n.52-14_52-10del
ENST00000599899.5:n.1416-14_1416-10del
ENST00000601008.1:c.242-1552_242-1548del	ENSP00000471384.1:n.242-1552_242-1548del
NM_000064.3:c.4457-14_4457-10del	NP_000055.2:n.4457-14_4457-10del
NM_000064.4:c.4457-14_4457-10del MANE Select	NP_000055.2:n.4457-14_4457-10del