Canonical Allele Identifier: CA10747896

Gene: CFHR4

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196912470G>C , CM000663.2:g.196912470G>C	GRCh38
NC_000001.10:g.196881600G>C , CM000663.1:g.196881600G>C	GRCh37
NC_000001.9:g.195148223G>C	NCBI36
NG_028159.1:g.29457G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699463.1:n.1066-270G>C
ENST00000608469.6:c.998-270G>C MANE Select	ENSP00000477162.2:n.998-270G>C
ENST00000251424.8:c.257-270G>C	ENSP00000251424.4:n.257-270G>C
ENST00000367416.6:c.995-270G>C	ENSP00000356386.2:n.995-270G>C
ENST00000367418.2:c.257-270G>C	ENSP00000356388.2:n.257-270G>C
ENST00000367421.4:c.59-36985G>C	ENSP00000356391.3:n.59-36985G>C
ENST00000608469.5:c.44-270G>C	ENSP00000477162.1:n.44-270G>C
NM_001201550.2:c.998-270G>C	NP_001188479.1:n.998-270G>C
NM_001201551.1:c.995-270G>C	NP_001188480.1:n.995-270G>C
NM_006684.4:c.257-270G>C	NP_006675.2:n.257-270G>C
XM_006711128.2:c.983-270G>C	XP_006711191.1:n.983-270G>C
XM_006711129.2:c.974-270G>C	XP_006711192.1:n.974-270G>C
XM_006711130.2:c.968-270G>C	XP_006711193.1:n.968-270G>C
XM_011509093.1:c.1013-270G>C	XP_011507395.1:n.1013-270G>C
XM_011509094.1:c.1013-270G>C	XP_011507396.1:n.1013-270G>C
XM_011509095.1:c.1013-270G>C	XP_011507397.1:n.1013-270G>C
XR_921727.1:n.1028-270G>C
XR_922396.1:n.591C>G
NM_001201550.3:c.998-270G>C MANE Select	NP_001188479.1:n.998-270G>C
XM_006711129.3:c.974-270G>C	XP_006711192.1:n.974-270G>C
XM_017000110.1:c.998-270G>C	XP_016855599.1:n.998-270G>C
XM_017000111.1:c.998-270G>C	XP_016855600.1:n.998-270G>C
XM_017000112.1:c.998-270G>C	XP_016855601.1:n.998-270G>C
XM_017000113.1:c.998-270G>C	XP_016855602.1:n.998-270G>C
XM_017000114.1:c.425-270G>C	XP_016855603.1:n.425-270G>C
XR_922396.2:n.610C>G
NM_001201551.2:c.995-270G>C	NP_001188480.1:n.995-270G>C
NM_006684.5:c.257-270G>C	NP_006675.2:n.257-270G>C