Canonical Allele Identifier: CA357854535

Gene: CFI

Linked Data

• gnomAD v4: 4-109741017-A-G
• COSMIC: COSM159966
• MyVariant Identifiers: chr4:g.110662173A>G (hg19) ; chr4:g.109741017A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.109741017A>G , CM000666.2:g.109741017A>G	GRCh38
NC_000004.11:g.110662173A>G , CM000666.1:g.110662173A>G	GRCh37
NC_000004.10:g.110881622A>G	NCBI36
NG_007569.1:g.65969T>C , LRG_48:g.65969T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695844.1:n.1713+1474T>C
ENST00000695845.1:n.1712+1474T>C
ENST00000695846.1:n.1652T>C
ENST00000394634.7:c.1628T>C MANE Select	ENSP00000378130.2:p.Val543Ala
ENST00000394635.8:c.1652T>C	ENSP00000378131.3:p.Val551Ala
ENST00000645635.1:c.1534+1474T>C	ENSP00000493607.1:n.1534+1474T>C
ENST00000394634.6:c.1628T>C	ENSP00000378130.2:p.Val543Ala
ENST00000394635.7:c.1652T>C	ENSP00000378131.3:p.Val551Ala
ENST00000504853.3:n.2045T>C
ENST00000512148.5:c.1607T>C	ENSP00000427438.1:p.Val536Ala
ENST00000618244.4:c.1045-212T>C	ENSP00000483416.1:n.1045-212T>C
NM_000204.3:c.1628T>C , LRG_48t1:c.1628T>C	NP_000195.2:p.Val543Ala
XM_005262975.1:c.1652T>C	XP_005263032.1:p.Val551Ala
XM_005262976.1:c.1607T>C	XP_005263033.1:p.Val536Ala
XM_006714209.1:c.1649T>C	XP_006714272.1:p.Val550Ala
XM_011531920.1:c.1558+1474T>C	XP_011530222.1:n.1558+1474T>C
NM_000204.4:c.1628T>C	NP_000195.2:p.Val543Ala
NM_001318057.1:c.1652T>C	NP_001304986.1:p.Val551Ala
NM_001331035.1:c.1607T>C	NP_001317964.1:p.Val536Ala
XM_011531920.2:c.1558+1474T>C	XP_011530222.1:n.1558+1474T>C
XM_017008164.2:c.1534+1474T>C	XP_016863653.1:n.1534+1474T>C
XM_017008165.2:c.1513+1474T>C	XP_016863654.1:n.1513+1474T>C
XM_017008166.2:c.1534+1474T>C	XP_016863655.1:n.1534+1474T>C
NM_001318057.2:c.1652T>C	NP_001304986.2:p.Val551Ala
NM_001331035.2:c.1607T>C	NP_001317964.1:p.Val536Ala
NM_001375278.1:c.1558+1474T>C	NP_001362207.1:n.1558+1474T>C
NM_001375279.1:c.1534+1474T>C	NP_001362208.1:n.1534+1474T>C
NM_001375280.1:c.1513+1474T>C	NP_001362209.1:n.1513+1474T>C
NM_001375281.1:c.1534+1474T>C	NP_001362210.1:n.1534+1474T>C
NM_001375282.1:c.1513+1474T>C	NP_001362211.1:n.1513+1474T>C
NM_001375283.1:c.1571T>C	NP_001362212.1:p.Val524Ala
NM_001375284.1:c.1019T>C	NP_001362213.1:p.Val340Ala
NR_164671.1:n.1375T>C
NR_164672.1:n.1678T>C
NR_164673.1:n.1652T>C
NM_000204.5:c.1628T>C MANE Select	NP_000195.3:p.Val543Ala