Canonical Allele Identifier: CA1876870714

Gene: C5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120974770T= , CM000671.2:g.120974770T=	GRCh38
NC_000009.11:g.123737048T= , CM000671.1:g.123737048T=	GRCh37
NC_000009.10:g.122776869T=	NCBI36
NG_007364.1:g.80507A= , LRG_28:g.80507A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.928+9A=
ENST00000696279.1:c.4337+9A=
ENST00000696280.1:n.4106+9A=
ENST00000696281.1:c.4035+9A=	ENSP00000512521.1:n.4035+9A=
ENST00000697921.1:n.2895+9A=
ENST00000697922.1:c.*4007+9A=	ENSP00000513478.1:n.*4007+9A=
ENST00000697923.1:n.4462+9A=
ENST00000223642.3:c.4017+9A= MANE Select	ENSP00000223642.1:n.4017+9A=
ENST00000223642.2:c.4017+9A=	ENSP00000223642.1:n.4017+9A=
NM_001735.2:c.4017+9A= , LRG_28t1:c.4017+9A=	NP_001726.2:n.4017+9A=
XM_011518980.1:c.4032+9A=	XP_011517282.1:n.4032+9A=
NM_001317163.1:c.4035+9A=	NP_001304092.1:n.4035+9A=
NM_001317163.2:c.4035+9A=	NP_001304092.1:n.4035+9A=
NM_001735.3:c.4017+9A= MANE Select	NP_001726.2:n.4017+9A=