Canonical Allele Identifier: CA1876865643

Gene: C5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120962282T= , CM000671.2:g.120962282T=	GRCh38
NC_000009.11:g.123724560T= , CM000671.1:g.123724560T=	GRCh37
NC_000009.10:g.122764381T=	NCBI36
NG_007364.1:g.92995A= , LRG_28:g.92995A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1538+389A=
ENST00000696279.1:c.4824+389A=
ENST00000696280.1:n.4593+389A=
ENST00000696281.1:c.4522+389A=	ENSP00000512521.1:n.4522+389A=
ENST00000697921.1:n.3382+389A=
ENST00000697922.1:c.*4494+389A=	ENSP00000513478.1:n.*4494+389A=
ENST00000697923.1:n.4949+389A=
ENST00000223642.3:c.4504+389A= MANE Select	ENSP00000223642.1:n.4504+389A=
ENST00000223642.2:c.4504+389A=	ENSP00000223642.1:n.4504+389A=
ENST00000480188.1:n.37+389A=
NM_001735.2:c.4504+389A= , LRG_28t1:c.4504+389A=	NP_001726.2:n.4504+389A=
XM_011518980.1:c.4519+389A=	XP_011517282.1:n.4519+389A=
NM_001317163.1:c.4522+389A=	NP_001304092.1:n.4522+389A=
NM_001317163.2:c.4522+389A=	NP_001304092.1:n.4522+389A=
NM_001735.3:c.4504+389A= MANE Select	NP_001726.2:n.4504+389A=