Canonical Allele Identifier: CA2691483614

Gene: C5

Linked Data

• gnomAD v4: 9-121006782-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.121006783del , CM000671.2:g.121006783del	GRCh38
NC_000009.11:g.123769061del , CM000671.1:g.123769061del	GRCh37
NC_000009.10:g.122808882del	NCBI36
NG_007364.1:g.48494del , LRG_28:g.48494del

Transcript Alleles

HGVS	Amino-acid change
ENST00000466280.2:c.1417+121del	ENSP00000513491.1:n.1417+121del
ENST00000696279.1:c.2742+121del
ENST00000696280.1:n.2511+121del
ENST00000696281.1:c.2440+121del	ENSP00000512521.1:n.2440+121del
ENST00000697921.1:n.1300+121del
ENST00000697922.1:c.*2412+121del	ENSP00000513478.1:n.*2412+121del
ENST00000697923.1:n.3027+121del
ENST00000223642.3:c.2422+121del MANE Select	ENSP00000223642.1:n.2422+121del
ENST00000223642.2:c.2422+121del	ENSP00000223642.1:n.2422+121del
ENST00000466280.1:n.25+121del
NM_001735.2:c.2422+121del , LRG_28t1:c.2422+121del	NP_001726.2:n.2422+121del
XM_011518980.1:c.2437+121del	XP_011517282.1:n.2437+121del
XM_011518981.1:c.2440+121del	XP_011517283.1:n.2440+121del
NM_001317163.1:c.2440+121del	NP_001304092.1:n.2440+121del
NM_001317164.1:c.2422+121del	NP_001304093.1:n.2422+121del
NM_001317163.2:c.2440+121del	NP_001304092.1:n.2440+121del
NM_001317164.2:c.2422+121del	NP_001304093.1:n.2422+121del
NM_001735.3:c.2422+121del MANE Select	NP_001726.2:n.2422+121del