Canonical Allele Identifier: CA2691480773

Gene: C5

Linked Data

• gnomAD v4: 9-120969056-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120969056C>T , CM000671.2:g.120969056C>T	GRCh38
NC_000009.11:g.123731334C>T , CM000671.1:g.123731334C>T	GRCh37
NC_000009.10:g.122771155C>T	NCBI36
NG_007364.1:g.86221G>A , LRG_28:g.86221G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000480188.2:n.1254+5G>A
ENST00000696279.1:c.4540+5G>A
ENST00000696280.1:n.4309+5G>A
ENST00000696281.1:c.4238+5G>A	ENSP00000512521.1:n.4238+5G>A
ENST00000697921.1:n.3098+5G>A
ENST00000697922.1:c.*4210+5G>A	ENSP00000513478.1:n.*4210+5G>A
ENST00000697923.1:n.4665+5G>A
ENST00000223642.3:c.4220+5G>A MANE Select	ENSP00000223642.1:n.4220+5G>A
ENST00000223642.2:c.4220+5G>A	ENSP00000223642.1:n.4220+5G>A
NM_001735.2:c.4220+5G>A , LRG_28t1:c.4220+5G>A	NP_001726.2:n.4220+5G>A
XM_011518980.1:c.4235+5G>A	XP_011517282.1:n.4235+5G>A
NM_001317163.1:c.4238+5G>A	NP_001304092.1:n.4238+5G>A
NM_001317163.2:c.4238+5G>A	NP_001304092.1:n.4238+5G>A
NM_001735.3:c.4220+5G>A MANE Select	NP_001726.2:n.4220+5G>A