Canonical Allele Identifier: CA1876874423

Gene: C5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120980540G= , CM000671.2:g.120980540G=	GRCh38
NC_000009.11:g.123742818G= , CM000671.1:g.123742818G=	GRCh37
NC_000009.10:g.122782639G=	NCBI36
NG_007364.1:g.74737C= , LRG_28:g.74737C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.398-286C=
ENST00000696279.1:c.3807-286C=
ENST00000696280.1:n.3576-286C=
ENST00000696281.1:c.3505-286C=	ENSP00000512521.1:n.3505-286C=
ENST00000697921.1:n.2365-286C=
ENST00000697922.1:c.*3477-286C=	ENSP00000513478.1:n.*3477-286C=
ENST00000697923.1:n.3932-286C=
ENST00000223642.3:c.3487-286C= MANE Select	ENSP00000223642.1:n.3487-286C=
ENST00000223642.2:c.3487-286C=	ENSP00000223642.1:n.3487-286C=
ENST00000489802.1:n.50-286C=
NM_001735.2:c.3487-286C= , LRG_28t1:c.3487-286C=	NP_001726.2:n.3487-286C=
XM_011518980.1:c.3502-286C=	XP_011517282.1:n.3502-286C=
NM_001317163.1:c.3505-286C=	NP_001304092.1:n.3505-286C=
NM_001317163.2:c.3505-286C=	NP_001304092.1:n.3505-286C=
NM_001735.3:c.3487-286C= MANE Select	NP_001726.2:n.3487-286C=