Canonical Allele Identifier: CA3246763

Gene: C9

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.39308257A>G , CM000667.2:g.39308257A>G	GRCh38
NC_000005.9:g.39308359A>G , CM000667.1:g.39308359A>G	GRCh37
NC_000005.8:g.39344116A>G	NCBI36
NG_009894.1:g.61297T>C , LRG_32:g.61297T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509186.6:c.1141T>C	ENSP00000512235.1:p.Cys381Arg
ENST00000695880.1:c.1112-1465T>C	ENSP00000512236.1:n.1112-1465T>C
ENST00000695881.1:c.1213T>C	ENSP00000512237.1:p.Cys405Arg
ENST00000695882.1:n.440T>C
ENST00000263408.5:c.1213T>C MANE Select	ENSP00000263408.4:p.Cys405Arg
ENST00000263408.4:c.1213T>C	ENSP00000263408.4:p.Cys405Arg
NM_001737.3:c.1213T>C , LRG_32t1:c.1213T>C	NP_001728.1:p.Cys405Arg
NM_001737.4:c.1213T>C	NP_001728.1:p.Cys405Arg
NM_001737.5:c.1213T>C MANE Select	NP_001728.1:p.Cys405Arg