Canonical Allele Identifier: CA2691480461

Gene: C5

Linked Data

• gnomAD v4: 9-120962837-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120962837G>T , CM000671.2:g.120962837G>T	GRCh38
NC_000009.11:g.123725115G>T , CM000671.1:g.123725115G>T	GRCh37
NC_000009.10:g.122764936G>T	NCBI36
NG_007364.1:g.92440C>A , LRG_28:g.92440C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1432+56C>A
ENST00000696279.1:c.4718+56C>A
ENST00000696280.1:n.4487+56C>A
ENST00000696281.1:c.4416+56C>A	ENSP00000512521.1:n.4416+56C>A
ENST00000697921.1:n.3276+56C>A
ENST00000697922.1:c.*4388+56C>A	ENSP00000513478.1:n.*4388+56C>A
ENST00000697923.1:n.4843+56C>A
ENST00000223642.3:c.4398+56C>A MANE Select	ENSP00000223642.1:n.4398+56C>A
ENST00000223642.2:c.4398+56C>A	ENSP00000223642.1:n.4398+56C>A
NM_001735.2:c.4398+56C>A , LRG_28t1:c.4398+56C>A	NP_001726.2:n.4398+56C>A
XM_011518980.1:c.4413+56C>A	XP_011517282.1:n.4413+56C>A
NM_001317163.1:c.4416+56C>A	NP_001304092.1:n.4416+56C>A
NM_001317163.2:c.4416+56C>A	NP_001304092.1:n.4416+56C>A
NM_001735.3:c.4398+56C>A MANE Select	NP_001726.2:n.4398+56C>A