Canonical Allele Identifier: CA2691480560

Gene: C5

Linked Data

• gnomAD v4: 9-120963119-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120963121del , CM000671.2:g.120963121del	GRCh38
NC_000009.11:g.123725399del , CM000671.1:g.123725399del	GRCh37
NC_000009.10:g.122765220del	NCBI36
NG_007364.1:g.92157del , LRG_28:g.92157del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1358-153del
ENST00000696279.1:c.4644-153del
ENST00000696280.1:n.4413-153del
ENST00000696281.1:c.4342-153del	ENSP00000512521.1:n.4342-153del
ENST00000697921.1:n.3202-153del
ENST00000697922.1:c.*4314-153del	ENSP00000513478.1:n.*4314-153del
ENST00000697923.1:n.4769-153del
ENST00000223642.3:c.4324-153del MANE Select	ENSP00000223642.1:n.4324-153del
ENST00000223642.2:c.4324-153del	ENSP00000223642.1:n.4324-153del
NM_001735.2:c.4324-153del , LRG_28t1:c.4324-153del	NP_001726.2:n.4324-153del
XM_011518980.1:c.4339-153del	XP_011517282.1:n.4339-153del
NM_001317163.1:c.4342-153del	NP_001304092.1:n.4342-153del
NM_001317163.2:c.4342-153del	NP_001304092.1:n.4342-153del
NM_001735.3:c.4324-153del MANE Select	NP_001726.2:n.4324-153del