Canonical Allele Identifier: CA2587871937

Gene: C3

Linked Data

• gnomAD v4: 19-6679594-G-GCATCTCCAGGTCT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679594_6679595insCATCTCCAGGTCT , CM000681.2:g.6679594_6679595insCATCTCCAGGTCT	GRCh38
NC_000019.9:g.6679605_6679606insCATCTCCAGGTCT , CM000681.1:g.6679605_6679606insCATCTCCAGGTCT	GRCh37
NC_000019.8:g.6630605_6630606insCATCTCCAGGTCT	NCBI36
NG_009557.1:g.46057_46058insAGACCTGGAGATG , LRG_27:g.46057_46058insAGACCTGGAGATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2805-99_2805-98insAGACCTGGAGATG
ENST00000695653.1:c.2366-99_2366-98insAGACCTGGAGATG	ENSP00000512084.1:n.2366-99_2366-98insAGACCTGGAGATG
ENST00000695654.1:c.3482-99_3482-98insAGACCTGGAGATG	ENSP00000512085.1:n.3482-99_3482-98insAGACCTGGAGATG
ENST00000695689.1:c.428-99_428-98insAGACCTGGAGATG	ENSP00000512101.1:n.428-99_428-98insAGACCTGGAGATG
ENST00000695690.1:n.1522-99_1522-98insAGACCTGGAGATG
ENST00000695691.1:n.1318-99_1318-98insAGACCTGGAGATG
ENST00000245907.11:c.4457-99_4457-98insAGACCTGGAGATG MANE Select	ENSP00000245907.4:n.4457-99_4457-98insAGACCTGGAGATG
ENST00000245907.10:c.4457-99_4457-98insAGACCTGGAGATG	ENSP00000245907.4:n.4457-99_4457-98insAGACCTGGAGATG
ENST00000599668.1:n.52-99_52-98insAGACCTGGAGATG
ENST00000599899.5:n.1416-99_1416-98insAGACCTGGAGATG
ENST00000601008.1:c.242-1637_242-1636insAGACCTGGAGATG	ENSP00000471384.1:n.242-1637_242-1636insAGACCTGGAGATG
NM_000064.3:c.4457-99_4457-98insAGACCTGGAGATG	NP_000055.2:n.4457-99_4457-98insAGACCTGGAGATG
NM_000064.4:c.4457-99_4457-98insAGACCTGGAGATG MANE Select	NP_000055.2:n.4457-99_4457-98insAGACCTGGAGATG