Canonical Allele Identifier: CA2516244235

Gene: C5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120954340_120954341insGGGGGGAGG , CM000671.2:g.120954340_120954341insGGGGGGAGG	GRCh38
NC_000009.11:g.123716618_123716619insGGGGGGAGG , CM000671.1:g.123716618_123716619insGGGGGGAGG	GRCh37
NC_000009.10:g.122756439_122756440insGGGGGGAGG	NCBI36
NG_007364.1:g.100936_100937insCCTCCCCCC , LRG_28:g.100936_100937insCCTCCCCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.4740_4741insCCTCCCCCC
ENST00000696279.1:c.5083-473_5083-472insCCTCCCCCC
ENST00000696280.1:n.4852-473_4852-472insCCTCCCCCC
ENST00000696281.1:c.4781-473_4781-472insCCTCCCCCC	ENSP00000512521.1:n.4781-473_4781-472insCCTCCCCCC
ENST00000697921.1:n.3641-473_3641-472insCCTCCCCCC
ENST00000697922.1:c.*4753-473_*4753-472insCCTCCCCCC	ENSP00000513478.1:n.*4753-473_*4753-472insCCTCCCCCC
ENST00000697923.1:n.8151_8152insCCTCCCCCC
ENST00000223642.3:c.4763-473_4763-472insCCTCCCCCC MANE Select	ENSP00000223642.1:n.4763-473_4763-472insCCTCCCCCC
ENST00000223642.2:c.4763-473_4763-472insCCTCCCCCC	ENSP00000223642.1:n.4763-473_4763-472insCCTCCCCCC
NM_001735.2:c.4763-473_4763-472insCCTCCCCCC , LRG_28t1:c.4763-473_4763-472insCCTCCCCCC	NP_001726.2:n.4763-473_4763-472insCCTCCCCCC
XM_011518980.1:c.4778-473_4778-472insCCTCCCCCC	XP_011517282.1:n.4778-473_4778-472insCCTCCCCCC
NM_001317163.1:c.4781-473_4781-472insCCTCCCCCC	NP_001304092.1:n.4781-473_4781-472insCCTCCCCCC
NM_001317163.2:c.4781-473_4781-472insCCTCCCCCC	NP_001304092.1:n.4781-473_4781-472insCCTCCCCCC
NM_001735.3:c.4763-473_4763-472insCCTCCCCCC MANE Select	NP_001726.2:n.4763-473_4763-472insCCTCCCCCC