Canonical Allele Identifier: CA1139786176

Gene: C1QA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22638465G= , CM000663.2:g.22638465G=	GRCh38
NC_000001.10:g.22964958G= , CM000663.1:g.22964958G=	GRCh37
NC_000001.9:g.22837545G=	NCBI36
NG_007282.1:g.6841G= , LRG_22:g.6841G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402322.2:c.164-368G=	ENSP00000385564.1:n.164-368G=
ENST00000438241.2:c.164-368G=	ENSP00000416841.2:n.164-368G=
ENST00000695738.1:c.-212-368G=	ENSP00000512131.1:n.-212-368G=
ENST00000695739.1:c.164-185G=	ENSP00000512132.1:n.164-185G=
ENST00000695740.1:c.164-368G=	ENSP00000512133.1:n.164-368G=
ENST00000695741.1:c.*83G=	ENSP00000512134.1:n.*83G=
ENST00000695742.1:c.*10G=	ENSP00000512135.1:n.*10G=
ENST00000695743.1:c.*340G=	ENSP00000512136.1:n.*340G=
ENST00000695744.1:c.164-368G=	ENSP00000512137.1:n.164-368G=
ENST00000695745.1:c.-580G=	ENSP00000512138.1:n.-580G=
ENST00000695746.1:c.164-185G=	ENSP00000512139.1:n.164-185G=
ENST00000695747.1:c.164-368G=	ENSP00000512140.1:n.164-368G=
ENST00000695748.1:c.164-368G=	ENSP00000512141.1:n.164-368G=
ENST00000374642.8:c.164-368G= MANE Select	ENSP00000363773.3:n.164-368G=
ENST00000374642.7:c.164-368G=	ENSP00000363773.3:n.164-368G=
ENST00000402322.1:c.164-368G=	ENSP00000385564.1:n.164-368G=
ENST00000438241.1:c.164-368G=	ENSP00000416841.1:n.164-368G=
NM_015991.2:c.164-368G= , LRG_22t1:c.164-368G=	NP_057075.1:n.164-368G=
NM_001347465.1:c.164-368G=	NP_001334394.1:n.164-368G=
NM_001347466.1:c.164-368G=	NP_001334395.1:n.164-368G=
NM_015991.3:c.164-368G=	NP_057075.1:n.164-368G=
NM_015991.4:c.164-368G= MANE Select	NP_057075.1:n.164-368G=
NM_001347465.2:c.164-368G=	NP_001334394.1:n.164-368G=
NM_001347466.2:c.164-368G=	NP_001334395.1:n.164-368G=