Canonical Allele Identifier: CA1876862568

Gene: C5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120954466_120954467delinsTG , CM000671.2:g.120954466_120954467delinsTG	GRCh38
NC_000009.11:g.123716744_123716745delinsTG , CM000671.1:g.123716744_123716745delinsTG	GRCh37
NC_000009.10:g.122756565_122756566delinsTG	NCBI36
NG_007364.1:g.100810_100811delinsCA , LRG_28:g.100810_100811delinsCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000480188.2:n.4614_4615delinsCA
ENST00000696279.1:c.5083-599_5083-598delinsCA
ENST00000696280.1:n.4852-599_4852-598delinsCA
ENST00000696281.1:c.4781-599_4781-598delinsCA	ENSP00000512521.1:n.4781-599_4781-598delinsCA
ENST00000697921.1:n.3641-599_3641-598delinsCA
ENST00000697922.1:c.*4753-599_*4753-598delinsCA	ENSP00000513478.1:n.*4753-599_*4753-598delinsCA
ENST00000697923.1:n.8025_8026delinsCA
ENST00000223642.3:c.4763-599_4763-598delinsCA MANE Select	ENSP00000223642.1:n.4763-599_4763-598delinsCA
ENST00000223642.2:c.4763-599_4763-598delinsCA	ENSP00000223642.1:n.4763-599_4763-598delinsCA
NM_001735.2:c.4763-599_4763-598delinsCA , LRG_28t1:c.4763-599_4763-598delinsCA	NP_001726.2:n.4763-599_4763-598delinsCA
XM_011518980.1:c.4778-599_4778-598delinsCA	XP_011517282.1:n.4778-599_4778-598delinsCA
NM_001317163.1:c.4781-599_4781-598delinsCA	NP_001304092.1:n.4781-599_4781-598delinsCA
NM_001317163.2:c.4781-599_4781-598delinsCA	NP_001304092.1:n.4781-599_4781-598delinsCA
NM_001735.3:c.4763-599_4763-598delinsCA MANE Select	NP_001726.2:n.4763-599_4763-598delinsCA