Canonical Allele Identifier: CA1876865804

Gene: C5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120962687G= , CM000671.2:g.120962687G=	GRCh38
NC_000009.11:g.123724965G= , CM000671.1:g.123724965G=	GRCh37
NC_000009.10:g.122764786G=	NCBI36
NG_007364.1:g.92590C= , LRG_28:g.92590C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1522C=
ENST00000696279.1:c.4808C=
ENST00000696280.1:n.4577C=
ENST00000696281.1:c.4506C=	ENSP00000512521.1:p.Tyr1502=
ENST00000697921.1:n.3366C=
ENST00000697922.1:c.*4478C=	ENSP00000513478.1:n.*4478C=
ENST00000697923.1:n.4933C=
ENST00000223642.3:c.4488C= MANE Select	ENSP00000223642.1:p.Tyr1496=
ENST00000223642.2:c.4488C=	ENSP00000223642.1:p.Tyr1496=
ENST00000480188.1:n.21C=
NM_001735.2:c.4488C= , LRG_28t1:c.4488C=	NP_001726.2:p.Tyr1496=
XM_011518980.1:c.4503C=	XP_011517282.1:p.Tyr1501=
NM_001317163.1:c.4506C=	NP_001304092.1:p.Tyr1502=
NM_001317163.2:c.4506C=	NP_001304092.1:p.Tyr1502=
NM_001735.3:c.4488C= MANE Select	NP_001726.2:p.Tyr1496=