Canonical Allele Identifier: CA440583657

Gene: CFI

Linked Data

• MyVariant Identifiers: chr4:g.110667451G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.109746295G>C , CM000666.2:g.109746295G>C	GRCh38
NC_000004.11:g.110667451G>C , CM000666.1:g.110667451G>C	GRCh37
NC_000004.10:g.110886900G>C	NCBI36
NG_007569.1:g.60691C>G , LRG_48:g.60691C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695844.1:n.1535C>G
ENST00000695845.1:n.1534C>G
ENST00000695846.1:n.1380C>G
ENST00000394634.7:c.1356C>G MANE Select	ENSP00000378130.2:p.Ala452=
ENST00000394635.8:c.1380C>G	ENSP00000378131.3:p.Ala460=
ENST00000645635.1:c.1356C>G	ENSP00000493607.1:p.Ala452=
ENST00000394634.6:c.1356C>G	ENSP00000378130.2:p.Ala452=
ENST00000394635.7:c.1380C>G	ENSP00000378131.3:p.Ala460=
ENST00000504853.3:n.1773C>G
ENST00000512148.5:c.1335C>G	ENSP00000427438.1:p.Ala445=
ENST00000618244.4:c.1044+3204C>G	ENSP00000483416.1:n.1044+3204C>G
NM_000204.3:c.1356C>G , LRG_48t1:c.1356C>G	NP_000195.2:p.Ala452=
XM_005262975.1:c.1380C>G	XP_005263032.1:p.Ala460=
XM_005262976.1:c.1335C>G	XP_005263033.1:p.Ala445=
XM_006714209.1:c.1377C>G	XP_006714272.1:p.Ala459=
XM_006714210.2:c.1380C>G	XP_006714273.1:p.Ala460=
XM_011531920.1:c.1380C>G	XP_011530222.1:p.Ala460=
NM_000204.4:c.1356C>G	NP_000195.2:p.Ala452=
NM_001318057.1:c.1380C>G	NP_001304986.1:p.Ala460=
NM_001331035.1:c.1335C>G	NP_001317964.1:p.Ala445=
XM_006714210.4:c.1380C>G	XP_006714273.1:p.Ala460=
XM_011531920.2:c.1380C>G	XP_011530222.1:p.Ala460=
XM_017008164.2:c.1356C>G	XP_016863653.1:p.Ala452=
XM_017008165.2:c.1335C>G	XP_016863654.1:p.Ala445=
XM_017008166.2:c.1356C>G	XP_016863655.1:p.Ala452=
NM_001318057.2:c.1380C>G	NP_001304986.2:p.Ala460=
NM_001331035.2:c.1335C>G	NP_001317964.1:p.Ala445=
NM_001375278.1:c.1380C>G	NP_001362207.1:p.Ala460=
NM_001375279.1:c.1356C>G	NP_001362208.1:p.Ala452=
NM_001375280.1:c.1335C>G	NP_001362209.1:p.Ala445=
NM_001375281.1:c.1356C>G	NP_001362210.1:p.Ala452=
NM_001375282.1:c.1335C>G	NP_001362211.1:p.Ala445=
NM_001375283.1:c.1299C>G	NP_001362212.1:p.Ala433=
NM_001375284.1:c.747C>G	NP_001362213.1:p.Ala249=
NR_164671.1:n.1176+2923C>G
NR_164672.1:n.1406C>G
NR_164673.1:n.1380C>G
NM_000204.5:c.1356C>G MANE Select	NP_000195.3:p.Ala452=