Canonical Allele Identifier: CA1876865964

Gene: C5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120963103_120963104delinsGA , CM000671.2:g.120963103_120963104delinsGA	GRCh38
NC_000009.11:g.123725381_123725382delinsGA , CM000671.1:g.123725381_123725382delinsGA	GRCh37
NC_000009.10:g.122765202_122765203delinsGA	NCBI36
NG_007364.1:g.92173_92174delinsTC , LRG_28:g.92173_92174delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1358-137_1358-136delinsTC
ENST00000696279.1:c.4644-137_4644-136delinsTC
ENST00000696280.1:n.4413-137_4413-136delinsTC
ENST00000696281.1:c.4342-137_4342-136delinsTC	ENSP00000512521.1:n.4342-137_4342-136delinsTC
ENST00000697921.1:n.3202-137_3202-136delinsTC
ENST00000697922.1:c.*4314-137_*4314-136delinsTC	ENSP00000513478.1:n.*4314-137_*4314-136delinsTC
ENST00000697923.1:n.4769-137_4769-136delinsTC
ENST00000223642.3:c.4324-137_4324-136delinsTC MANE Select	ENSP00000223642.1:n.4324-137_4324-136delinsTC
ENST00000223642.2:c.4324-137_4324-136delinsTC	ENSP00000223642.1:n.4324-137_4324-136delinsTC
NM_001735.2:c.4324-137_4324-136delinsTC , LRG_28t1:c.4324-137_4324-136delinsTC	NP_001726.2:n.4324-137_4324-136delinsTC
XM_011518980.1:c.4339-137_4339-136delinsTC	XP_011517282.1:n.4339-137_4339-136delinsTC
NM_001317163.1:c.4342-137_4342-136delinsTC	NP_001304092.1:n.4342-137_4342-136delinsTC
NM_001317163.2:c.4342-137_4342-136delinsTC	NP_001304092.1:n.4342-137_4342-136delinsTC
NM_001735.3:c.4324-137_4324-136delinsTC MANE Select	NP_001726.2:n.4324-137_4324-136delinsTC