Canonical Allele Identifier: CA1876865871

Gene: C5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120962867_120962868delinsGA , CM000671.2:g.120962867_120962868delinsGA	GRCh38
NC_000009.11:g.123725145_123725146delinsGA , CM000671.1:g.123725145_123725146delinsGA	GRCh37
NC_000009.10:g.122764966_122764967delinsGA	NCBI36
NG_007364.1:g.92409_92410delinsTC , LRG_28:g.92409_92410delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1432+25_1432+26delinsTC
ENST00000696279.1:c.4718+25_4718+26delinsTC
ENST00000696280.1:n.4487+25_4487+26delinsTC
ENST00000696281.1:c.4416+25_4416+26delinsTC	ENSP00000512521.1:n.4416+25_4416+26delinsTC
ENST00000697921.1:n.3276+25_3276+26delinsTC
ENST00000697922.1:c.*4388+25_*4388+26delinsTC	ENSP00000513478.1:n.*4388+25_*4388+26delinsTC
ENST00000697923.1:n.4843+25_4843+26delinsTC
ENST00000223642.3:c.4398+25_4398+26delinsTC MANE Select	ENSP00000223642.1:n.4398+25_4398+26delinsTC
ENST00000223642.2:c.4398+25_4398+26delinsTC	ENSP00000223642.1:n.4398+25_4398+26delinsTC
NM_001735.2:c.4398+25_4398+26delinsTC , LRG_28t1:c.4398+25_4398+26delinsTC	NP_001726.2:n.4398+25_4398+26delinsTC
XM_011518980.1:c.4413+25_4413+26delinsTC	XP_011517282.1:n.4413+25_4413+26delinsTC
NM_001317163.1:c.4416+25_4416+26delinsTC	NP_001304092.1:n.4416+25_4416+26delinsTC
NM_001317163.2:c.4416+25_4416+26delinsTC	NP_001304092.1:n.4416+25_4416+26delinsTC
NM_001735.3:c.4398+25_4398+26delinsTC MANE Select	NP_001726.2:n.4398+25_4398+26delinsTC