Canonical Allele Identifier: CA1876889309

Gene: C5

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.121019492G>T , CM000671.2:g.121019492G>T	GRCh38
NC_000009.11:g.123781770G>T , CM000671.1:g.123781770G>T	GRCh37
NC_000009.10:g.122821591G>T	NCBI36
NG_007364.1:g.35785C>A , LRG_28:g.35785C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466280.2:c.501+484C>A	ENSP00000513491.1:n.501+484C>A
ENST00000696279.1:c.1826+484C>A
ENST00000696280.1:n.1595+484C>A
ENST00000696281.1:c.1524+484C>A	ENSP00000512521.1:n.1524+484C>A
ENST00000697922.1:c.*1496+484C>A	ENSP00000513478.1:n.*1496+484C>A
ENST00000697923.1:n.2111+484C>A
ENST00000223642.3:c.1506+484C>A MANE Select	ENSP00000223642.1:n.1506+484C>A
ENST00000223642.2:c.1506+484C>A	ENSP00000223642.1:n.1506+484C>A
NM_001735.2:c.1506+484C>A , LRG_28t1:c.1506+484C>A	NP_001726.2:n.1506+484C>A
XM_011518980.1:c.1521+484C>A	XP_011517282.1:n.1521+484C>A
XM_011518981.1:c.1524+484C>A	XP_011517283.1:n.1524+484C>A
NM_001317163.1:c.1524+484C>A	NP_001304092.1:n.1524+484C>A
NM_001317164.1:c.1506+484C>A	NP_001304093.1:n.1506+484C>A
NM_001317163.2:c.1524+484C>A	NP_001304092.1:n.1524+484C>A
NM_001317164.2:c.1506+484C>A	NP_001304093.1:n.1506+484C>A
NM_001735.3:c.1506+484C>A MANE Select	NP_001726.2:n.1506+484C>A