Canonical Allele Identifier: CA1876865918

Gene: C5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120962982_120962983delinsAG , CM000671.2:g.120962982_120962983delinsAG	GRCh38
NC_000009.11:g.123725260_123725261delinsAG , CM000671.1:g.123725260_123725261delinsAG	GRCh37
NC_000009.10:g.122765081_122765082delinsAG	NCBI36
NG_007364.1:g.92294_92295delinsCT , LRG_28:g.92294_92295delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1358-16_1358-15delinsCT
ENST00000696279.1:c.4644-16_4644-15delinsCT
ENST00000696280.1:n.4413-16_4413-15delinsCT
ENST00000696281.1:c.4342-16_4342-15delinsCT	ENSP00000512521.1:n.4342-16_4342-15delinsCT
ENST00000697921.1:n.3202-16_3202-15delinsCT
ENST00000697922.1:c.*4314-16_*4314-15delinsCT	ENSP00000513478.1:n.*4314-16_*4314-15delinsCT
ENST00000697923.1:n.4769-16_4769-15delinsCT
ENST00000223642.3:c.4324-16_4324-15delinsCT MANE Select	ENSP00000223642.1:n.4324-16_4324-15delinsCT
ENST00000223642.2:c.4324-16_4324-15delinsCT	ENSP00000223642.1:n.4324-16_4324-15delinsCT
NM_001735.2:c.4324-16_4324-15delinsCT , LRG_28t1:c.4324-16_4324-15delinsCT	NP_001726.2:n.4324-16_4324-15delinsCT
XM_011518980.1:c.4339-16_4339-15delinsCT	XP_011517282.1:n.4339-16_4339-15delinsCT
NM_001317163.1:c.4342-16_4342-15delinsCT	NP_001304092.1:n.4342-16_4342-15delinsCT
NM_001317163.2:c.4342-16_4342-15delinsCT	NP_001304092.1:n.4342-16_4342-15delinsCT
NM_001735.3:c.4324-16_4324-15delinsCT MANE Select	NP_001726.2:n.4324-16_4324-15delinsCT