Canonical Allele Identifier: CA1876865792

Gene: C5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120962655_120962656delinsGC , CM000671.2:g.120962655_120962656delinsGC	GRCh38
NC_000009.11:g.123724933_123724934delinsGC , CM000671.1:g.123724933_123724934delinsGC	GRCh37
NC_000009.10:g.122764754_122764755delinsGC	NCBI36
NG_007364.1:g.92621_92622delinsGC , LRG_28:g.92621_92622delinsGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000480188.2:n.1538+15_1538+16delinsGC
ENST00000696279.1:c.4824+15_4824+16delinsGC
ENST00000696280.1:n.4593+15_4593+16delinsGC
ENST00000696281.1:c.4522+15_4522+16delinsGC	ENSP00000512521.1:n.4522+15_4522+16delins...
ENST00000697921.1:n.3382+15_3382+16delinsGC
ENST00000697922.1:c.*4494+15_*4494+16delinsGC	ENSP00000513478.1:n.*4494+15_*4494+16deli...
ENST00000697923.1:n.4949+15_4949+16delinsGC
ENST00000223642.3:c.4504+15_4504+16delinsGC MANE Select	ENSP00000223642.1:n.4504+15_4504+16delins...
ENST00000223642.2:c.4504+15_4504+16delinsGC	ENSP00000223642.1:n.4504+15_4504+16delins...
ENST00000480188.1:n.37+15_37+16delinsGC
NM_001735.2:c.4504+15_4504+16delinsGC , LRG_28t1:c.4504+15_4504+16delinsGC	NP_001726.2:n.4504+15_4504+16delinsGC
XM_011518980.1:c.4519+15_4519+16delinsGC	XP_011517282.1:n.4519+15_4519+16delinsGC
NM_001317163.1:c.4522+15_4522+16delinsGC	NP_001304092.1:n.4522+15_4522+16delinsGC
NM_001317163.2:c.4522+15_4522+16delinsGC	NP_001304092.1:n.4522+15_4522+16delinsGC
NM_001735.3:c.4504+15_4504+16delinsGC MANE Select	NP_001726.2:n.4504+15_4504+16delinsGC