Canonical Allele Identifier: CA1876874339

Gene: C5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120980430A= , CM000671.2:g.120980430A=	GRCh38
NC_000009.11:g.123742708A= , CM000671.1:g.123742708A=	GRCh37
NC_000009.10:g.122782529A=	NCBI36
NG_007364.1:g.74847T= , LRG_28:g.74847T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000480188.2:n.398-176T=
ENST00000696279.1:c.3807-176T=
ENST00000696280.1:n.3576-176T=
ENST00000696281.1:c.3505-176T=	ENSP00000512521.1:n.3505-176T=
ENST00000697921.1:n.2365-176T=
ENST00000697922.1:c.*3477-176T=	ENSP00000513478.1:n.*3477-176T=
ENST00000697923.1:n.3932-176T=
ENST00000223642.3:c.3487-176T= MANE Select	ENSP00000223642.1:n.3487-176T=
ENST00000223642.2:c.3487-176T=	ENSP00000223642.1:n.3487-176T=
ENST00000489802.1:n.50-176T=
NM_001735.2:c.3487-176T= , LRG_28t1:c.3487-176T=	NP_001726.2:n.3487-176T=
XM_011518980.1:c.3502-176T=	XP_011517282.1:n.3502-176T=
NM_001317163.1:c.3505-176T=	NP_001304092.1:n.3505-176T=
NM_001317163.2:c.3505-176T=	NP_001304092.1:n.3505-176T=
NM_001735.3:c.3487-176T= MANE Select	NP_001726.2:n.3487-176T=