Canonical Allele Identifier: CA1876862586

Gene: C5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120954533_120954535delinsCTT , CM000671.2:g.120954533_120954535delinsCTT	GRCh38
NC_000009.11:g.123716811_123716813delinsCTT , CM000671.1:g.123716811_123716813delinsCTT	GRCh37
NC_000009.10:g.122756632_122756634delinsCTT	NCBI36
NG_007364.1:g.100742_100744delinsAAG , LRG_28:g.100742_100744delinsAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.4546_4548delinsAAG
ENST00000696279.1:c.5083-667_5083-665delinsAAG
ENST00000696280.1:n.4852-667_4852-665delinsAAG
ENST00000696281.1:c.4781-667_4781-665delinsAAG	ENSP00000512521.1:n.4781-667_4781-665delinsAAG
ENST00000697921.1:n.3641-667_3641-665delinsAAG
ENST00000697922.1:c.*4753-667_*4753-665delinsAAG	ENSP00000513478.1:n.*4753-667_*4753-665delinsAAG
ENST00000697923.1:n.7957_7959delinsAAG
ENST00000223642.3:c.4763-667_4763-665delinsAAG MANE Select	ENSP00000223642.1:n.4763-667_4763-665delinsAAG
ENST00000223642.2:c.4763-667_4763-665delinsAAG	ENSP00000223642.1:n.4763-667_4763-665delinsAAG
NM_001735.2:c.4763-667_4763-665delinsAAG , LRG_28t1:c.4763-667_4763-665delinsAAG	NP_001726.2:n.4763-667_4763-665delinsAAG
XM_011518980.1:c.4778-667_4778-665delinsAAG	XP_011517282.1:n.4778-667_4778-665delinsAAG
NM_001317163.1:c.4781-667_4781-665delinsAAG	NP_001304092.1:n.4781-667_4781-665delinsAAG
NM_001317163.2:c.4781-667_4781-665delinsAAG	NP_001304092.1:n.4781-667_4781-665delinsAAG
NM_001735.3:c.4763-667_4763-665delinsAAG MANE Select	NP_001726.2:n.4763-667_4763-665delinsAAG