Canonical Allele Identifier: CA2587871910

Gene: C3

Linked Data

• gnomAD v4: 19-6679564-CCAGATCCCCAGTTCTCAGTCTTCAGACCTGGAGATGCTAGGTCTTCAACCCCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679573_6679625del , CM000681.2:g.6679573_6679625del	GRCh38
NC_000019.9:g.6679584_6679636del , CM000681.1:g.6679584_6679636del	GRCh37
NC_000019.8:g.6630584_6630636del	NCBI36
NG_009557.1:g.46035_46087del , LRG_27:g.46035_46087del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2805-121_2805-69del
ENST00000695653.1:c.2366-121_2366-69del	ENSP00000512084.1:n.2366-121_2366-69del
ENST00000695654.1:c.3482-121_3482-69del	ENSP00000512085.1:n.3482-121_3482-69del
ENST00000695689.1:c.428-121_428-69del	ENSP00000512101.1:n.428-121_428-69del
ENST00000695690.1:n.1522-121_1522-69del
ENST00000695691.1:n.1318-121_1318-69del
ENST00000245907.11:c.4457-121_4457-69del MANE Select	ENSP00000245907.4:n.4457-121_4457-69del
ENST00000245907.10:c.4457-121_4457-69del	ENSP00000245907.4:n.4457-121_4457-69del
ENST00000599668.1:n.52-121_52-69del
ENST00000599899.5:n.1416-121_1416-69del
ENST00000601008.1:c.242-1659_242-1607del	ENSP00000471384.1:n.242-1659_242-1607del
NM_000064.3:c.4457-121_4457-69del	NP_000055.2:n.4457-121_4457-69del
NM_000064.4:c.4457-121_4457-69del MANE Select	NP_000055.2:n.4457-121_4457-69del