Canonical Allele Identifier: CA859584676

Gene: C5

Linked Data

• dbSNP Id: rs892818443
• gnomAD v3: 9-120980599-C-CA
• gnomAD v4: 9-120980599-C-CA
• MyVariant Identifiers: chr9:g.123742877_123742878insA (hg19) ; chr9:g.120980599_120980600insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120980599_120980600insA , CM000671.2:g.120980599_120980600insA	GRCh38
NC_000009.11:g.123742877_123742878insA , CM000671.1:g.123742877_123742878insA	GRCh37
NC_000009.10:g.122782698_122782699insA	NCBI36
NG_007364.1:g.74677_74678insT , LRG_28:g.74677_74678insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.398-346_398-345insT
ENST00000696279.1:c.3807-346_3807-345insT
ENST00000696280.1:n.3576-346_3576-345insT
ENST00000696281.1:c.3505-346_3505-345insT	ENSP00000512521.1:n.3505-346_3505-345insT
ENST00000697921.1:n.2365-346_2365-345insT
ENST00000697922.1:c.*3477-346_*3477-345insT	ENSP00000513478.1:n.*3477-346_*3477-345insT
ENST00000697923.1:n.3932-346_3932-345insT
ENST00000223642.3:c.3487-346_3487-345insT MANE Select	ENSP00000223642.1:n.3487-346_3487-345insT
ENST00000223642.2:c.3487-346_3487-345insT	ENSP00000223642.1:n.3487-346_3487-345insT
ENST00000489802.1:n.50-346_50-345insT
NM_001735.2:c.3487-346_3487-345insT , LRG_28t1:c.3487-346_3487-345insT	NP_001726.2:n.3487-346_3487-345insT
XM_011518980.1:c.3502-346_3502-345insT	XP_011517282.1:n.3502-346_3502-345insT
NM_001317163.1:c.3505-346_3505-345insT	NP_001304092.1:n.3505-346_3505-345insT
NM_001317163.2:c.3505-346_3505-345insT	NP_001304092.1:n.3505-346_3505-345insT
NM_001735.3:c.3487-346_3487-345insT MANE Select	NP_001726.2:n.3487-346_3487-345insT