Canonical Allele Identifier: CA103694300

Gene: CFI

Linked Data

• dbSNP Id: rs886996561
• MyVariant Identifiers: chr4:g.110678739_110678740del (hg19) ; chr4:g.109757583_109757584del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.109757586_109757587del , CM000666.2:g.109757586_109757587del	GRCh38
NC_000004.11:g.110678742_110678743del , CM000666.1:g.110678742_110678743del	GRCh37
NC_000004.10:g.110898191_110898192del	NCBI36
NG_007569.1:g.49402_49403del , LRG_48:g.49402_49403del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695844.1:n.1083+179_1083+180del
ENST00000695845.1:n.1082+179_1082+180del
ENST00000695846.1:n.928+179_928+180del
ENST00000394634.7:c.904+179_904+180del MANE Select	ENSP00000378130.2:n.904+179_904+180del
ENST00000394635.8:c.928+179_928+180del	ENSP00000378131.3:n.928+179_928+180del
ENST00000645635.1:c.904+179_904+180del	ENSP00000493607.1:n.904+179_904+180del
ENST00000394634.6:c.904+179_904+180del	ENSP00000378130.2:n.904+179_904+180del
ENST00000394635.7:c.928+179_928+180del	ENSP00000378131.3:n.928+179_928+180del
ENST00000504853.3:n.1321+179_1321+180del
ENST00000512148.5:c.883+2686_883+2687del	ENSP00000427438.1:n.883+2686_883+2687del
ENST00000618244.4:c.904+179_904+180del	ENSP00000483416.1:n.904+179_904+180del
NM_000204.3:c.904+179_904+180del , LRG_48t1:c.904+179_904+180del	NP_000195.2:n.904+179_904+180del
XM_005262975.1:c.928+179_928+180del	XP_005263032.1:n.928+179_928+180del
XM_005262976.1:c.883+2686_883+2687del	XP_005263033.1:n.883+2686_883+2687del
XM_006714209.1:c.925+179_925+180del	XP_006714272.1:n.925+179_925+180del
XM_006714210.2:c.928+179_928+180del	XP_006714273.1:n.928+179_928+180del
XM_011531920.1:c.928+179_928+180del	XP_011530222.1:n.928+179_928+180del
NM_000204.4:c.904+179_904+180del	NP_000195.2:n.904+179_904+180del
NM_001318057.1:c.928+179_928+180del	NP_001304986.1:n.928+179_928+180del
NM_001331035.1:c.883+2686_883+2687del	NP_001317964.1:n.883+2686_883+2687del
XM_006714210.4:c.928+179_928+180del	XP_006714273.1:n.928+179_928+180del
XM_011531920.2:c.928+179_928+180del	XP_011530222.1:n.928+179_928+180del
XM_017008164.2:c.904+179_904+180del	XP_016863653.1:n.904+179_904+180del
XM_017008165.2:c.883+2686_883+2687del	XP_016863654.1:n.883+2686_883+2687del
XM_017008166.2:c.904+179_904+180del	XP_016863655.1:n.904+179_904+180del
NM_001318057.2:c.928+179_928+180del	NP_001304986.2:n.928+179_928+180del
NM_001331035.2:c.883+2686_883+2687del	NP_001317964.1:n.883+2686_883+2687del
NM_001375278.1:c.928+179_928+180del	NP_001362207.1:n.928+179_928+180del
NM_001375279.1:c.904+179_904+180del	NP_001362208.1:n.904+179_904+180del
NM_001375280.1:c.883+2686_883+2687del	NP_001362209.1:n.883+2686_883+2687del
NM_001375281.1:c.904+179_904+180del	NP_001362210.1:n.904+179_904+180del
NM_001375282.1:c.883+2686_883+2687del	NP_001362211.1:n.883+2686_883+2687del
NM_001375283.1:c.883+2686_883+2687del	NP_001362212.1:n.883+2686_883+2687del
NM_001375284.1:c.295+179_295+180del	NP_001362213.1:n.295+179_295+180del
NR_164671.1:n.932+179_932+180del
NR_164672.1:n.956+179_956+180del
NR_164673.1:n.932+179_932+180del
NM_000204.5:c.904+179_904+180del MANE Select	NP_000195.3:n.904+179_904+180del