Canonical Allele Identifier: CA1876884221

Gene: C5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.121006722_121006723delinsAG , CM000671.2:g.121006722_121006723delinsAG	GRCh38
NC_000009.11:g.123769000_123769001delinsAG , CM000671.1:g.123769000_123769001delinsAG	GRCh37
NC_000009.10:g.122808821_122808822delinsAG	NCBI36
NG_007364.1:g.48554_48555delinsCT , LRG_28:g.48554_48555delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000466280.2:c.1417+181_1417+182delinsCT	ENSP00000513491.1:n.1417+181_1417+182delinsCT
ENST00000696279.1:c.2742+181_2742+182delinsCT
ENST00000696280.1:n.2511+181_2511+182delinsCT
ENST00000696281.1:c.2440+181_2440+182delinsCT	ENSP00000512521.1:n.2440+181_2440+182delinsCT
ENST00000697921.1:n.1300+181_1300+182delinsCT
ENST00000697922.1:c.*2412+181_*2412+182delinsCT	ENSP00000513478.1:n.*2412+181_*2412+182delinsCT
ENST00000697923.1:n.3027+181_3027+182delinsCT
ENST00000223642.3:c.2422+181_2422+182delinsCT MANE Select	ENSP00000223642.1:n.2422+181_2422+182delinsCT
ENST00000223642.2:c.2422+181_2422+182delinsCT	ENSP00000223642.1:n.2422+181_2422+182delinsCT
ENST00000466280.1:n.25+181_25+182delinsCT
NM_001735.2:c.2422+181_2422+182delinsCT , LRG_28t1:c.2422+181_2422+182delinsCT	NP_001726.2:n.2422+181_2422+182delinsCT
XM_011518980.1:c.2437+181_2437+182delinsCT	XP_011517282.1:n.2437+181_2437+182delinsCT
XM_011518981.1:c.2440+181_2440+182delinsCT	XP_011517283.1:n.2440+181_2440+182delinsCT
NM_001317163.1:c.2440+181_2440+182delinsCT	NP_001304092.1:n.2440+181_2440+182delinsCT
NM_001317164.1:c.2422+181_2422+182delinsCT	NP_001304093.1:n.2422+181_2422+182delinsCT
NM_001317163.2:c.2440+181_2440+182delinsCT	NP_001304092.1:n.2440+181_2440+182delinsCT
NM_001317164.2:c.2422+181_2422+182delinsCT	NP_001304093.1:n.2422+181_2422+182delinsCT
NM_001735.3:c.2422+181_2422+182delinsCT MANE Select	NP_001726.2:n.2422+181_2422+182delinsCT