Canonical Allele Identifier: CA2579437639

Gene: C5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120969161A>G , CM000671.2:g.120969161A>G	GRCh38
NC_000009.11:g.123731439A>G , CM000671.1:g.123731439A>G	GRCh37
NC_000009.10:g.122771260A>G	NCBI36
NG_007364.1:g.86116T>C , LRG_28:g.86116T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1197-43T>C
ENST00000696279.1:c.4483-43T>C
ENST00000696280.1:n.4252-43T>C
ENST00000696281.1:c.4181-43T>C	ENSP00000512521.1:n.4181-43T>C
ENST00000697921.1:n.3041-43T>C
ENST00000697922.1:c.*4153-43T>C	ENSP00000513478.1:n.*4153-43T>C
ENST00000697923.1:n.4608-43T>C
ENST00000223642.3:c.4163-43T>C MANE Select	ENSP00000223642.1:n.4163-43T>C
ENST00000223642.2:c.4163-43T>C	ENSP00000223642.1:n.4163-43T>C
NM_001735.2:c.4163-43T>C , LRG_28t1:c.4163-43T>C	NP_001726.2:n.4163-43T>C
XM_011518980.1:c.4178-43T>C	XP_011517282.1:n.4178-43T>C
NM_001317163.1:c.4181-43T>C	NP_001304092.1:n.4181-43T>C
NM_001317163.2:c.4181-43T>C	NP_001304092.1:n.4181-43T>C
NM_001735.3:c.4163-43T>C MANE Select	NP_001726.2:n.4163-43T>C