Canonical Allele Identifier: CA1876865870

Gene: C5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120962864A= , CM000671.2:g.120962864A=	GRCh38
NC_000009.11:g.123725142A= , CM000671.1:g.123725142A=	GRCh37
NC_000009.10:g.122764963A=	NCBI36
NG_007364.1:g.92413T= , LRG_28:g.92413T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1432+29T=
ENST00000696279.1:c.4718+29T=
ENST00000696280.1:n.4487+29T=
ENST00000696281.1:c.4416+29T=	ENSP00000512521.1:n.4416+29T=
ENST00000697921.1:n.3276+29T=
ENST00000697922.1:c.*4388+29T=	ENSP00000513478.1:n.*4388+29T=
ENST00000697923.1:n.4843+29T=
ENST00000223642.3:c.4398+29T= MANE Select	ENSP00000223642.1:n.4398+29T=
ENST00000223642.2:c.4398+29T=	ENSP00000223642.1:n.4398+29T=
NM_001735.2:c.4398+29T= , LRG_28t1:c.4398+29T=	NP_001726.2:n.4398+29T=
XM_011518980.1:c.4413+29T=	XP_011517282.1:n.4413+29T=
NM_001317163.1:c.4416+29T=	NP_001304092.1:n.4416+29T=
NM_001317163.2:c.4416+29T=	NP_001304092.1:n.4416+29T=
NM_001735.3:c.4398+29T= MANE Select	NP_001726.2:n.4398+29T=