Canonical Allele Identifier: CA2320568063

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713670_6713671delinsCA , CM000681.2:g.6713670_6713671delinsCA	GRCh38
NC_000019.9:g.6713681_6713682delinsCA , CM000681.1:g.6713681_6713682delinsCA	GRCh37
NC_000019.8:g.6664681_6664682delinsCA	NCBI36
NG_009557.1:g.11981_11982delinsTG , LRG_27:g.11981_11982delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.651-162_651-161delinsTG	ENSP00000512083.1:n.651-162_651-161delinsTG
ENST00000245907.11:c.774-162_774-161delinsTG MANE Select	ENSP00000245907.4:n.774-162_774-161delinsTG
ENST00000245907.10:c.774-162_774-161delinsTG	ENSP00000245907.4:n.774-162_774-161delinsTG
ENST00000595577.1:n.278-162_278-161delinsTG
ENST00000597442.5:n.23+95_23+96delinsTG
NM_000064.3:c.774-162_774-161delinsTG	NP_000055.2:n.774-162_774-161delinsTG
NM_000064.4:c.774-162_774-161delinsTG MANE Select	NP_000055.2:n.774-162_774-161delinsTG