Canonical Allele Identifier: CA440818733

Gene: CFI

Linked Data

• MyVariant Identifiers: chr4:g.110662169C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.109741013C>A , CM000666.2:g.109741013C>A	GRCh38
NC_000004.11:g.110662169C>A , CM000666.1:g.110662169C>A	GRCh37
NC_000004.10:g.110881618C>A	NCBI36
NG_007569.1:g.65973G>T , LRG_48:g.65973G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695844.1:n.1713+1478G>T
ENST00000695845.1:n.1712+1478G>T
ENST00000695846.1:n.1656G>T
ENST00000394634.7:c.1632G>T MANE Select	ENSP00000378130.2:p.Val544=
ENST00000394635.8:c.1656G>T	ENSP00000378131.3:p.Val552=
ENST00000645635.1:c.1534+1478G>T	ENSP00000493607.1:n.1534+1478G>T
ENST00000394634.6:c.1632G>T	ENSP00000378130.2:p.Val544=
ENST00000394635.7:c.1656G>T	ENSP00000378131.3:p.Val552=
ENST00000504853.3:n.2049G>T
ENST00000512148.5:c.1611G>T	ENSP00000427438.1:p.Val537=
ENST00000618244.4:c.1045-208G>T	ENSP00000483416.1:n.1045-208G>T
NM_000204.3:c.1632G>T , LRG_48t1:c.1632G>T	NP_000195.2:p.Val544=
XM_005262975.1:c.1656G>T	XP_005263032.1:p.Val552=
XM_005262976.1:c.1611G>T	XP_005263033.1:p.Val537=
XM_006714209.1:c.1653G>T	XP_006714272.1:p.Val551=
XM_011531920.1:c.1558+1478G>T	XP_011530222.1:n.1558+1478G>T
NM_000204.4:c.1632G>T	NP_000195.2:p.Val544=
NM_001318057.1:c.1656G>T	NP_001304986.1:p.Val552=
NM_001331035.1:c.1611G>T	NP_001317964.1:p.Val537=
XM_011531920.2:c.1558+1478G>T	XP_011530222.1:n.1558+1478G>T
XM_017008164.2:c.1534+1478G>T	XP_016863653.1:n.1534+1478G>T
XM_017008165.2:c.1513+1478G>T	XP_016863654.1:n.1513+1478G>T
XM_017008166.2:c.1534+1478G>T	XP_016863655.1:n.1534+1478G>T
NM_001318057.2:c.1656G>T	NP_001304986.2:p.Val552=
NM_001331035.2:c.1611G>T	NP_001317964.1:p.Val537=
NM_001375278.1:c.1558+1478G>T	NP_001362207.1:n.1558+1478G>T
NM_001375279.1:c.1534+1478G>T	NP_001362208.1:n.1534+1478G>T
NM_001375280.1:c.1513+1478G>T	NP_001362209.1:n.1513+1478G>T
NM_001375281.1:c.1534+1478G>T	NP_001362210.1:n.1534+1478G>T
NM_001375282.1:c.1513+1478G>T	NP_001362211.1:n.1513+1478G>T
NM_001375283.1:c.1575G>T	NP_001362212.1:p.Val525=
NM_001375284.1:c.1023G>T	NP_001362213.1:p.Val341=
NR_164671.1:n.1379G>T
NR_164672.1:n.1682G>T
NR_164673.1:n.1656G>T
NM_000204.5:c.1632G>T MANE Select	NP_000195.3:p.Val544=