Canonical Allele Identifier: CA2579437579

Gene: C5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120962660G>A , CM000671.2:g.120962660G>A	GRCh38
NC_000009.11:g.123724938G>A , CM000671.1:g.123724938G>A	GRCh37
NC_000009.10:g.122764759G>A	NCBI36
NG_007364.1:g.92617C>T , LRG_28:g.92617C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000480188.2:n.1538+11C>T
ENST00000696279.1:c.4824+11C>T
ENST00000696280.1:n.4593+11C>T
ENST00000696281.1:c.4522+11C>T	ENSP00000512521.1:n.4522+11C>T
ENST00000697921.1:n.3382+11C>T
ENST00000697922.1:c.*4494+11C>T	ENSP00000513478.1:n.*4494+11C>T
ENST00000697923.1:n.4949+11C>T
ENST00000223642.3:c.4504+11C>T MANE Select	ENSP00000223642.1:n.4504+11C>T
ENST00000223642.2:c.4504+11C>T	ENSP00000223642.1:n.4504+11C>T
ENST00000480188.1:n.37+11C>T
NM_001735.2:c.4504+11C>T , LRG_28t1:c.4504+11C>T	NP_001726.2:n.4504+11C>T
XM_011518980.1:c.4519+11C>T	XP_011517282.1:n.4519+11C>T
NM_001317163.1:c.4522+11C>T	NP_001304092.1:n.4522+11C>T
NM_001317163.2:c.4522+11C>T	NP_001304092.1:n.4522+11C>T
NM_001735.3:c.4504+11C>T MANE Select	NP_001726.2:n.4504+11C>T