Canonical Allele Identifier: CA2691480520
Gene: C5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.120963070_120963071insG , CM000671.2:g.120963070_120963071insG GRCh38
NC_000009.11:g.123725348_123725349insG , CM000671.1:g.123725348_123725349insG GRCh37
NC_000009.10:g.122765169_122765170insG NCBI36
NG_007364.1:g.92206_92207insC , LRG_28:g.92206_92207insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000480188.2:n.1358-104_1358-103insC
ENST00000696279.1:c.4644-104_4644-103insC
ENST00000696280.1:n.4413-104_4413-103insC
ENST00000696281.1:c.4342-104_4342-103insC ENSP00000512521.1:n.4342-104_4342-103insC
ENST00000697921.1:n.3202-104_3202-103insC
ENST00000697922.1:c.*4314-104_*4314-103insC ENSP00000513478.1:n.*4314-104_*4314-103insC
ENST00000697923.1:n.4769-104_4769-103insC
ENST00000223642.3:c.4324-104_4324-103insC MANE Select ENSP00000223642.1:n.4324-104_4324-103insC
ENST00000223642.2:c.4324-104_4324-103insC ENSP00000223642.1:n.4324-104_4324-103insC
NM_001735.2:c.4324-104_4324-103insC , LRG_28t1:c.4324-104_4324-103insC NP_001726.2:n.4324-104_4324-103insC
XM_011518980.1:c.4339-104_4339-103insC XP_011517282.1:n.4339-104_4339-103insC
NM_001317163.1:c.4342-104_4342-103insC NP_001304092.1:n.4342-104_4342-103insC
NM_001317163.2:c.4342-104_4342-103insC NP_001304092.1:n.4342-104_4342-103insC
NM_001735.3:c.4324-104_4324-103insC MANE Select NP_001726.2:n.4324-104_4324-103insC