Canonical Allele Identifier: CA374746212

Gene: C5

Linked Data

• MyVariant Identifiers: chr9:g.123724978G>A (hg19) ; chr9:g.120962700G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120962700G>A , CM000671.2:g.120962700G>A	GRCh38
NC_000009.11:g.123724978G>A , CM000671.1:g.123724978G>A	GRCh37
NC_000009.10:g.122764799G>A	NCBI36
NG_007364.1:g.92577C>T , LRG_28:g.92577C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1509C>T
ENST00000696279.1:c.4795C>T
ENST00000696280.1:n.4564C>T
ENST00000696281.1:c.4493C>T	ENSP00000512521.1:p.Thr1498Ile
ENST00000697921.1:n.3353C>T
ENST00000697922.1:c.*4465C>T	ENSP00000513478.1:n.*4465C>T
ENST00000697923.1:n.4920C>T
ENST00000223642.3:c.4475C>T MANE Select	ENSP00000223642.1:p.Thr1492Ile
ENST00000223642.2:c.4475C>T	ENSP00000223642.1:p.Thr1492Ile
ENST00000480188.1:n.8C>T
NM_001735.2:c.4475C>T , LRG_28t1:c.4475C>T	NP_001726.2:p.Thr1492Ile
XM_011518980.1:c.4490C>T	XP_011517282.1:p.Thr1497Ile
NM_001317163.1:c.4493C>T	NP_001304092.1:p.Thr1498Ile
NM_001317163.2:c.4493C>T	NP_001304092.1:p.Thr1498Ile
NM_001735.3:c.4475C>T MANE Select	NP_001726.2:p.Thr1492Ile