Canonical Allele Identifier: CA2320550598

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679818_6679819delinsAT , CM000681.2:g.6679818_6679819delinsAT	GRCh38
NC_000019.9:g.6679829_6679830delinsAT , CM000681.1:g.6679829_6679830delinsAT	GRCh37
NC_000019.8:g.6630829_6630830delinsAT	NCBI36
NG_009557.1:g.45833_45834delinsAT , LRG_27:g.45833_45834delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2805-323_2805-322delinsAT
ENST00000695653.1:c.2366-323_2366-322delinsAT	ENSP00000512084.1:n.2366-323_2366-322delinsAT
ENST00000695654.1:c.3482-323_3482-322delinsAT	ENSP00000512085.1:n.3482-323_3482-322delinsAT
ENST00000695689.1:c.428-323_428-322delinsAT	ENSP00000512101.1:n.428-323_428-322delinsAT
ENST00000695690.1:n.1522-323_1522-322delinsAT
ENST00000695691.1:n.1318-323_1318-322delinsAT
ENST00000245907.11:c.4457-323_4457-322delinsAT MANE Select	ENSP00000245907.4:n.4457-323_4457-322delinsAT
ENST00000245907.10:c.4457-323_4457-322delinsAT	ENSP00000245907.4:n.4457-323_4457-322delinsAT
ENST00000599668.1:n.51+282_51+283delinsAT
ENST00000599899.5:n.1416-323_1416-322delinsAT
ENST00000601008.1:c.242-1861_242-1860delinsAT	ENSP00000471384.1:n.242-1861_242-1860delinsAT
NM_000064.3:c.4457-323_4457-322delinsAT	NP_000055.2:n.4457-323_4457-322delinsAT
NM_000064.4:c.4457-323_4457-322delinsAT MANE Select	NP_000055.2:n.4457-323_4457-322delinsAT