Canonical Allele Identifier: CA2320568173

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713780_6713781delinsCA , CM000681.2:g.6713780_6713781delinsCA	GRCh38
NC_000019.9:g.6713791_6713792delinsCA , CM000681.1:g.6713791_6713792delinsCA	GRCh37
NC_000019.8:g.6664791_6664792delinsCA	NCBI36
NG_009557.1:g.11871_11872delinsTG , LRG_27:g.11871_11872delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.650+211_650+212delinsTG	ENSP00000512083.1:n.650+211_650+212delinsTG
ENST00000245907.11:c.773+211_773+212delinsTG MANE Select	ENSP00000245907.4:n.773+211_773+212delinsTG
ENST00000245907.10:c.773+211_773+212delinsTG	ENSP00000245907.4:n.773+211_773+212delinsTG
ENST00000595577.1:n.277+211_277+212delinsTG
ENST00000597442.5:n.8_9delinsTG
NM_000064.3:c.773+211_773+212delinsTG	NP_000055.2:n.773+211_773+212delinsTG
NM_000064.4:c.773+211_773+212delinsTG MANE Select	NP_000055.2:n.773+211_773+212delinsTG