Canonical Allele Identifier: CA2014394408

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.7091477T= , CM000674.2:g.7091477T= GRCh38
NC_000012.11:g.7244073T= , CM000674.1:g.7244073T= GRCh37
NC_000012.10:g.7135214T= NCBI36
NG_062465.1:g.6131A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647956.2:c.206A= (C1R) MANE Select ENSP00000497341.1:p.Glu69=
ENST00000535233.6:c.206A= (C1R) ENSP00000438636.3:p.Glu69=
ENST00000536053.6:c.248A= (C1R) ENSP00000444271.3:p.Glu83=
ENST00000536092.1:n.311A= (C1R)
ENST00000538050.5:c.-110A= (C1R) ENSP00000444009.1:n.-110A=
ENST00000539803.5:c.673A= (C1RL)
ENST00000540242.2:c.206A= (C1R) ENSP00000442946.1:p.Glu69=
ENST00000540394.5:n.965A= (C1R)
ENST00000540610.5:c.-85+910A= (C1R) ENSP00000439223.1:n.-85+910A=
ENST00000541042.5:c.-110A= (C1R) ENSP00000441601.1:n.-110A=
ENST00000542285.5:c.206A= (C1R) ENSP00000438615.2:p.Glu69=
ENST00000543362.5:c.206A= (C1R) ENSP00000446356.1:p.Glu69=
ENST00000543835.5:c.206A= (C1R) ENSP00000445285.1:p.Glu69=
ENST00000545466.1:n.259A= (C1R)
NM_001733.4:c.206A= (C1R) NP_001724.3:p.Glu69=
NM_001354346.1:c.248A= (C1R) NP_001341275.1:p.Glu83=
NM_001733.6:c.206A= (C1R) NP_001724.4:p.Glu69=
NM_001733.7:c.206A= (C1R) MANE Select NP_001724.4:p.Glu69=
NM_001354346.2:c.248A= (C1R) NP_001341275.1:p.Glu83=