Canonical Allele Identifier: CA1139776757

Gene: C1QA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22638945A= , CM000663.2:g.22638945A=	GRCh38
NC_000001.10:g.22965438A= , CM000663.1:g.22965438A=	GRCh37
NC_000001.9:g.22838025A=	NCBI36
NG_007282.1:g.7321A= , LRG_22:g.7321A=
NG_007565.1:g.321A= , LRG_24:g.321A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402322.2:c.276A=	ENSP00000385564.1:p.Gly92=
ENST00000438241.2:c.276A=	ENSP00000416841.2:p.Gly92=
ENST00000695738.1:c.-100A=	ENSP00000512131.1:n.-100A=
ENST00000695739.1:c.*270A=	ENSP00000512132.1:n.*270A=
ENST00000695740.1:c.276A=	ENSP00000512133.1:p.Gly92=
ENST00000695741.1:c.*563A=	ENSP00000512134.1:n.*563A=
ENST00000695742.1:c.*490A=	ENSP00000512135.1:n.*490A=
ENST00000695743.1:c.*820A=	ENSP00000512136.1:n.*820A=
ENST00000695744.1:c.276A=	ENSP00000512137.1:p.Gly92=
ENST00000695745.1:c.-100A=	ENSP00000512138.1:n.-100A=
ENST00000695746.1:c.*270A=	ENSP00000512139.1:n.*270A=
ENST00000695747.1:c.276A=	ENSP00000512140.1:p.Gly92=
ENST00000695748.1:c.276A=	ENSP00000512141.1:p.Gly92=
ENST00000374642.8:c.276A= MANE Select	ENSP00000363773.3:p.Gly92=
ENST00000374642.7:c.276A=	ENSP00000363773.3:p.Gly92=
ENST00000402322.1:c.276A=	ENSP00000385564.1:p.Gly92=
ENST00000438241.1:c.276A=	ENSP00000416841.1:p.Gly92=
NM_015991.2:c.276A= , LRG_22t1:c.276A=	NP_057075.1:p.Gly92=
NM_001347465.1:c.276A=	NP_001334394.1:p.Gly92=
NM_001347466.1:c.276A=	NP_001334395.1:p.Gly92=
NM_015991.3:c.276A=	NP_057075.1:p.Gly92=
NM_015991.4:c.276A= MANE Select	NP_057075.1:p.Gly92=
NM_001347465.2:c.276A=	NP_001334394.1:p.Gly92=
NM_001347466.2:c.276A=	NP_001334395.1:p.Gly92=