Canonical Allele Identifier: CA1876868397

Gene: C5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120969108G= , CM000671.2:g.120969108G=	GRCh38
NC_000009.11:g.123731386G= , CM000671.1:g.123731386G=	GRCh37
NC_000009.10:g.122771207G=	NCBI36
NG_007364.1:g.86169C= , LRG_28:g.86169C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1207C=
ENST00000696279.1:c.4493C=
ENST00000696280.1:n.4262C=
ENST00000696281.1:c.4191C=	ENSP00000512521.1:p.Tyr1397=
ENST00000697921.1:n.3051C=
ENST00000697922.1:c.*4163C=	ENSP00000513478.1:n.*4163C=
ENST00000697923.1:n.4618C=
ENST00000223642.3:c.4173C= MANE Select	ENSP00000223642.1:p.Tyr1391=
ENST00000223642.2:c.4173C=	ENSP00000223642.1:p.Tyr1391=
NM_001735.2:c.4173C= , LRG_28t1:c.4173C=	NP_001726.2:p.Tyr1391=
XM_011518980.1:c.4188C=	XP_011517282.1:p.Tyr1396=
NM_001317163.1:c.4191C=	NP_001304092.1:p.Tyr1397=
NM_001317163.2:c.4191C=	NP_001304092.1:p.Tyr1397=
NM_001735.3:c.4173C= MANE Select	NP_001726.2:p.Tyr1391=