Canonical Allele Identifier: CA2587875465

Gene: C3

Linked Data

• gnomAD v4: 19-6697870-T-TGCGG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697870_6697871insGCGG , CM000681.2:g.6697870_6697871insGCGG	GRCh38
NC_000019.9:g.6697881_6697882insGCGG , CM000681.1:g.6697881_6697882insGCGG	GRCh37
NC_000019.8:g.6648881_6648882insGCGG	NCBI36
NG_009557.1:g.27781_27782insCCGC , LRG_27:g.27781_27782insCCGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.789-77_789-76insCCGC
ENST00000695652.1:c.2318-77_2318-76insCCGC	ENSP00000512083.1:n.2318-77_2318-76insCCGC
ENST00000695653.1:c.350-77_350-76insCCGC	ENSP00000512084.1:n.350-77_350-76insCCGC
ENST00000695654.1:c.1565-77_1565-76insCCGC	ENSP00000512085.1:n.1565-77_1565-76insCCGC
ENST00000695655.1:c.1382-77_1382-76insCCGC	ENSP00000512086.1:n.1382-77_1382-76insCCGC
ENST00000695692.1:n.1805-77_1805-76insCCGC
ENST00000245907.11:c.2441-77_2441-76insCCGC MANE Select	ENSP00000245907.4:n.2441-77_2441-76insCCGC
ENST00000245907.10:c.2441-77_2441-76insCCGC	ENSP00000245907.4:n.2441-77_2441-76insCCGC
ENST00000602053.1:n.489-77_489-76insCCGC
NM_000064.3:c.2441-77_2441-76insCCGC	NP_000055.2:n.2441-77_2441-76insCCGC
NM_000064.4:c.2441-77_2441-76insCCGC MANE Select	NP_000055.2:n.2441-77_2441-76insCCGC