Canonical Allele Identifier: CA1876865811

Gene: C5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120962705A= , CM000671.2:g.120962705A=	GRCh38
NC_000009.11:g.123724983A= , CM000671.1:g.123724983A=	GRCh37
NC_000009.10:g.122764804A=	NCBI36
NG_007364.1:g.92572T= , LRG_28:g.92572T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1504T=
ENST00000696279.1:c.4790T=
ENST00000696280.1:n.4559T=
ENST00000696281.1:c.4488T=	ENSP00000512521.1:p.Pro1496=
ENST00000697921.1:n.3348T=
ENST00000697922.1:c.*4460T=	ENSP00000513478.1:n.*4460T=
ENST00000697923.1:n.4915T=
ENST00000223642.3:c.4470T= MANE Select	ENSP00000223642.1:p.Pro1490=
ENST00000223642.2:c.4470T=	ENSP00000223642.1:p.Pro1490=
ENST00000480188.1:n.3T=
NM_001735.2:c.4470T= , LRG_28t1:c.4470T=	NP_001726.2:p.Pro1490=
XM_011518980.1:c.4485T=	XP_011517282.1:p.Pro1495=
NM_001317163.1:c.4488T=	NP_001304092.1:p.Pro1496=
NM_001317163.2:c.4488T=	NP_001304092.1:p.Pro1496=
NM_001735.3:c.4470T= MANE Select	NP_001726.2:p.Pro1490=