Canonical Allele Identifier: CA374747608

Gene: C5

Linked Data

• MyVariant Identifiers: chr9:g.123725217G>C (hg19) ; chr9:g.120962939G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120962939G>C , CM000671.2:g.120962939G>C	GRCh38
NC_000009.11:g.123725217G>C , CM000671.1:g.123725217G>C	GRCh37
NC_000009.10:g.122765038G>C	NCBI36
NG_007364.1:g.92338C>G , LRG_28:g.92338C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1386C>G
ENST00000696279.1:c.4672C>G
ENST00000696280.1:n.4441C>G
ENST00000696281.1:c.4370C>G	ENSP00000512521.1:p.Thr1457Ser
ENST00000697921.1:n.3230C>G
ENST00000697922.1:c.*4342C>G	ENSP00000513478.1:n.*4342C>G
ENST00000697923.1:n.4797C>G
ENST00000223642.3:c.4352C>G MANE Select	ENSP00000223642.1:p.Thr1451Ser
ENST00000223642.2:c.4352C>G	ENSP00000223642.1:p.Thr1451Ser
NM_001735.2:c.4352C>G , LRG_28t1:c.4352C>G	NP_001726.2:p.Thr1451Ser
XM_011518980.1:c.4367C>G	XP_011517282.1:p.Thr1456Ser
NM_001317163.1:c.4370C>G	NP_001304092.1:p.Thr1457Ser
NM_001317163.2:c.4370C>G	NP_001304092.1:p.Thr1457Ser
NM_001735.3:c.4352C>G MANE Select	NP_001726.2:p.Thr1451Ser