Canonical Allele Identifier: CA374746512

Gene: C5

Linked Data

• MyVariant Identifiers: chr9:g.123725005A>G (hg19) ; chr9:g.120962727A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120962727A>G , CM000671.2:g.120962727A>G	GRCh38
NC_000009.11:g.123725005A>G , CM000671.1:g.123725005A>G	GRCh37
NC_000009.10:g.122764826A>G	NCBI36
NG_007364.1:g.92550T>C , LRG_28:g.92550T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1482T>C
ENST00000696279.1:c.4768T>C
ENST00000696280.1:n.4537T>C
ENST00000696281.1:c.4466T>C	ENSP00000512521.1:p.Phe1489Ser
ENST00000697921.1:n.3326T>C
ENST00000697922.1:c.*4438T>C	ENSP00000513478.1:n.*4438T>C
ENST00000697923.1:n.4893T>C
ENST00000223642.3:c.4448T>C MANE Select	ENSP00000223642.1:p.Phe1483Ser
ENST00000223642.2:c.4448T>C	ENSP00000223642.1:p.Phe1483Ser
NM_001735.2:c.4448T>C , LRG_28t1:c.4448T>C	NP_001726.2:p.Phe1483Ser
XM_011518980.1:c.4463T>C	XP_011517282.1:p.Phe1488Ser
NM_001317163.1:c.4466T>C	NP_001304092.1:p.Phe1489Ser
NM_001317163.2:c.4466T>C	NP_001304092.1:p.Phe1489Ser
NM_001735.3:c.4448T>C MANE Select	NP_001726.2:p.Phe1483Ser