Canonical Allele Identifier: CA1876865861

Gene: C5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120962851A= , CM000671.2:g.120962851A=	GRCh38
NC_000009.11:g.123725129A= , CM000671.1:g.123725129A=	GRCh37
NC_000009.10:g.122764950A=	NCBI36
NG_007364.1:g.92426T= , LRG_28:g.92426T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1432+42T=
ENST00000696279.1:c.4718+42T=
ENST00000696280.1:n.4487+42T=
ENST00000696281.1:c.4416+42T=	ENSP00000512521.1:n.4416+42T=
ENST00000697921.1:n.3276+42T=
ENST00000697922.1:c.*4388+42T=	ENSP00000513478.1:n.*4388+42T=
ENST00000697923.1:n.4843+42T=
ENST00000223642.3:c.4398+42T= MANE Select	ENSP00000223642.1:n.4398+42T=
ENST00000223642.2:c.4398+42T=	ENSP00000223642.1:n.4398+42T=
NM_001735.2:c.4398+42T= , LRG_28t1:c.4398+42T=	NP_001726.2:n.4398+42T=
XM_011518980.1:c.4413+42T=	XP_011517282.1:n.4413+42T=
NM_001317163.1:c.4416+42T=	NP_001304092.1:n.4416+42T=
NM_001317163.2:c.4416+42T=	NP_001304092.1:n.4416+42T=
NM_001735.3:c.4398+42T= MANE Select	NP_001726.2:n.4398+42T=