Canonical Allele Identifier: CA2511813128

Gene: C5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120954335_120954336insG , CM000671.2:g.120954335_120954336insG	GRCh38
NC_000009.11:g.123716613_123716614insG , CM000671.1:g.123716613_123716614insG	GRCh37
NC_000009.10:g.122756434_122756435insG	NCBI36
NG_007364.1:g.100941_100942insC , LRG_28:g.100941_100942insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.4745_4746insC
ENST00000696279.1:c.5083-468_5083-467insC
ENST00000696280.1:n.4852-468_4852-467insC
ENST00000696281.1:c.4781-468_4781-467insC	ENSP00000512521.1:n.4781-468_4781-467insC
ENST00000697921.1:n.3641-468_3641-467insC
ENST00000697922.1:c.*4753-468_*4753-467insC	ENSP00000513478.1:n.*4753-468_*4753-467insC
ENST00000697923.1:n.8156_8157insC
ENST00000223642.3:c.4763-468_4763-467insC MANE Select	ENSP00000223642.1:n.4763-468_4763-467insC
ENST00000223642.2:c.4763-468_4763-467insC	ENSP00000223642.1:n.4763-468_4763-467insC
NM_001735.2:c.4763-468_4763-467insC , LRG_28t1:c.4763-468_4763-467insC	NP_001726.2:n.4763-468_4763-467insC
XM_011518980.1:c.4778-468_4778-467insC	XP_011517282.1:n.4778-468_4778-467insC
NM_001317163.1:c.4781-468_4781-467insC	NP_001304092.1:n.4781-468_4781-467insC
NM_001317163.2:c.4781-468_4781-467insC	NP_001304092.1:n.4781-468_4781-467insC
NM_001735.3:c.4763-468_4763-467insC MANE Select	NP_001726.2:n.4763-468_4763-467insC