Canonical Allele Identifier: CA559064966

Gene: C9

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.39306607C>T , CM000667.2:g.39306607C>T	GRCh38
NC_000005.9:g.39306709C>T , CM000667.1:g.39306709C>T	GRCh37
NC_000005.8:g.39342466C>T	NCBI36
NG_009894.1:g.62947G>A , LRG_32:g.62947G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001737.5:c.1416+10G>A MANE Select	NP_001728.1:n.1416+10G>A
ENST00000263408.5:c.1416+10G>A MANE Select	ENSP00000263408.4:n.1416+10G>A
NM_001737.3:c.1416+10G>A , LRG_32t1:c.1416+10G>A	NP_001728.1:n.1416+10G>A
NM_001737.4:c.1416+10G>A	NP_001728.1:n.1416+10G>A
ENST00000263408.4:c.1416+10G>A	ENSP00000263408.4:n.1416+10G>A
ENST00000509186.6:c.1344+10G>A	ENSP00000512235.1:n.1344+10G>A
ENST00000695880.1:c.1287+10G>A	ENSP00000512236.1:n.1287+10G>A
ENST00000695881.1:c.1416+10G>A	ENSP00000512237.1:n.1416+10G>A
ENST00000695882.1:n.643+10G>A