Canonical Allele Identifier: CA2320566021

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709941_6709942delinsTG , CM000681.2:g.6709941_6709942delinsTG	GRCh38
NC_000019.9:g.6709952_6709953delinsTG , CM000681.1:g.6709952_6709953delinsTG	GRCh37
NC_000019.8:g.6660952_6660953delinsTG	NCBI36
NG_009557.1:g.15710_15711delinsCA , LRG_27:g.15710_15711delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-100_1564-99delinsCA	ENSP00000512083.1:n.1564-100_1564-99delinsCA
ENST00000695654.1:c.811-100_811-99delinsCA	ENSP00000512085.1:n.811-100_811-99delinsCA
ENST00000695655.1:c.592-64_592-63delinsCA	ENSP00000512086.1:n.592-64_592-63delinsCA
ENST00000695692.1:n.1051-100_1051-99delinsCA
ENST00000245907.11:c.1687-100_1687-99delinsCA MANE Select	ENSP00000245907.4:n.1687-100_1687-99delinsCA
ENST00000245907.10:c.1687-100_1687-99delinsCA	ENSP00000245907.4:n.1687-100_1687-99delinsCA
ENST00000600763.1:n.320-100_320-99delinsCA
NM_000064.3:c.1687-100_1687-99delinsCA	NP_000055.2:n.1687-100_1687-99delinsCA
NM_000064.4:c.1687-100_1687-99delinsCA MANE Select	NP_000055.2:n.1687-100_1687-99delinsCA