Canonical Allele Identifier: CA374747834

Gene: C5

Linked Data

• gnomAD v4: 9-120962955-C-G
• MyVariant Identifiers: chr9:g.123725233C>G (hg19) ; chr9:g.120962955C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120962955C>G , CM000671.2:g.120962955C>G	GRCh38
NC_000009.11:g.123725233C>G , CM000671.1:g.123725233C>G	GRCh37
NC_000009.10:g.122765054C>G	NCBI36
NG_007364.1:g.92322G>C , LRG_28:g.92322G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1370G>C
ENST00000696279.1:c.4656G>C
ENST00000696280.1:n.4425G>C
ENST00000696281.1:c.4354G>C	ENSP00000512521.1:p.Val1452Leu
ENST00000697921.1:n.3214G>C
ENST00000697922.1:c.*4326G>C	ENSP00000513478.1:n.*4326G>C
ENST00000697923.1:n.4781G>C
ENST00000223642.3:c.4336G>C MANE Select	ENSP00000223642.1:p.Val1446Leu
ENST00000223642.2:c.4336G>C	ENSP00000223642.1:p.Val1446Leu
NM_001735.2:c.4336G>C , LRG_28t1:c.4336G>C	NP_001726.2:p.Val1446Leu
XM_011518980.1:c.4351G>C	XP_011517282.1:p.Val1451Leu
NM_001317163.1:c.4354G>C	NP_001304092.1:p.Val1452Leu
NM_001317163.2:c.4354G>C	NP_001304092.1:p.Val1452Leu
NM_001735.3:c.4336G>C MANE Select	NP_001726.2:p.Val1446Leu