Canonical Allele Identifier: CA374746604

Gene: C5

Linked Data

• MyVariant Identifiers: chr9:g.123725018T>C (hg19) ; chr9:g.120962740T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120962740T>C , CM000671.2:g.120962740T>C	GRCh38
NC_000009.11:g.123725018T>C , CM000671.1:g.123725018T>C	GRCh37
NC_000009.10:g.122764839T>C	NCBI36
NG_007364.1:g.92537A>G , LRG_28:g.92537A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1469A>G
ENST00000696279.1:c.4755A>G
ENST00000696280.1:n.4524A>G
ENST00000696281.1:c.4453A>G	ENSP00000512521.1:p.Ile1485Val
ENST00000697921.1:n.3313A>G
ENST00000697922.1:c.*4425A>G	ENSP00000513478.1:n.*4425A>G
ENST00000697923.1:n.4880A>G
ENST00000223642.3:c.4435A>G MANE Select	ENSP00000223642.1:p.Ile1479Val
ENST00000223642.2:c.4435A>G	ENSP00000223642.1:p.Ile1479Val
NM_001735.2:c.4435A>G , LRG_28t1:c.4435A>G	NP_001726.2:p.Ile1479Val
XM_011518980.1:c.4450A>G	XP_011517282.1:p.Ile1484Val
NM_001317163.1:c.4453A>G	NP_001304092.1:p.Ile1485Val
NM_001317163.2:c.4453A>G	NP_001304092.1:p.Ile1485Val
NM_001735.3:c.4435A>G MANE Select	NP_001726.2:p.Ile1479Val