Canonical Allele Identifier: CA2832508837

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713829_6713830del , CM000681.2:g.6713829_6713830del	GRCh38
NC_000019.9:g.6713840_6713841del , CM000681.1:g.6713840_6713841del	GRCh37
NC_000019.8:g.6664840_6664841del	NCBI36
NG_009557.1:g.11822_11823del , LRG_27:g.11822_11823del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.650+162_650+163del	ENSP00000512083.1:n.650+162_650+163del
ENST00000245907.11:c.773+162_773+163del MANE Select	ENSP00000245907.4:n.773+162_773+163del
ENST00000245907.10:c.773+162_773+163del	ENSP00000245907.4:n.773+162_773+163del
ENST00000595577.1:n.277+162_277+163del
NM_000064.3:c.773+162_773+163del	NP_000055.2:n.773+162_773+163del
NM_000064.4:c.773+162_773+163del MANE Select	NP_000055.2:n.773+162_773+163del