Canonical Allele Identifier: CA1593291

Gene: CLIP4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29167482A>G , CM000664.2:g.29167482A>G	GRCh38
NC_000002.11:g.29390348A>G , CM000664.1:g.29390348A>G	GRCh37
NC_000002.10:g.29243852A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481628.2:n.241A>G
ENST00000493551.2:n.1862A>G
ENST00000685126.1:c.*1560A>G	ENSP00000510353.1:n.*1560A>G
ENST00000686125.1:c.1665A>G	ENSP00000509057.1:p.Thr555=
ENST00000686470.1:c.*672A>G	ENSP00000509047.1:n.*672A>G
ENST00000686848.1:c.1665A>G	ENSP00000509281.1:p.Thr555=
ENST00000687104.1:c.1254A>G	ENSP00000508721.1:p.Thr418=
ENST00000687166.1:c.*232A>G	ENSP00000510523.1:n.*232A>G
ENST00000687450.1:c.1461A>G	ENSP00000508879.1:p.Thr487=
ENST00000687506.1:c.1686A>G	ENSP00000509486.1:p.Thr562=
ENST00000687889.1:c.1078+10135A>G	ENSP00000510043.1:n.1078+10135A>G
ENST00000687915.1:c.*232A>G	ENSP00000509578.1:n.*232A>G
ENST00000688724.1:c.*232A>G	ENSP00000510594.1:n.*232A>G
ENST00000689017.1:c.1530A>G	ENSP00000510497.1:p.Thr510=
ENST00000689045.1:n.1833A>G
ENST00000689070.1:c.1665A>G	ENSP00000509643.1:p.Thr555=
ENST00000689605.1:c.1665A>G	ENSP00000508948.1:p.Thr555=
ENST00000690063.1:c.1665A>G	ENSP00000508552.1:p.Thr555=
ENST00000690615.1:c.*232A>G	ENSP00000508511.1:n.*232A>G
ENST00000691129.1:c.1665A>G	ENSP00000510138.1:p.Thr555=
ENST00000691341.1:c.*2A>G	ENSP00000510119.1:n.*2A>G
ENST00000691509.1:n.1856A>G
ENST00000691796.1:c.1344A>G	ENSP00000509274.1:p.Thr448=
ENST00000691852.1:n.1760A>G
ENST00000693041.1:c.*2A>G	ENSP00000508782.1:n.*2A>G
ENST00000693232.1:n.1584A>G
ENST00000693264.1:c.1665A>G	ENSP00000509159.1:p.Thr555=
ENST00000693446.1:c.*617A>G	ENSP00000510153.1:n.*617A>G
ENST00000693482.1:n.847A>G
ENST00000693513.1:c.*2A>G	ENSP00000510678.1:n.*2A>G
ENST00000693694.1:c.*306A>G	ENSP00000510549.1:n.*306A>G
ENST00000320081.10:c.1665A>G MANE Select	ENSP00000327009.5:p.Thr555=
ENST00000320081.9:c.1665A>G	ENSP00000327009.5:p.Thr555=
ENST00000401605.5:c.1665A>G	ENSP00000384242.1:p.Thr555=
ENST00000401617.6:c.1344A>G	ENSP00000385148.2:p.Thr448=
ENST00000404424.5:c.1665A>G	ENSP00000385594.1:p.Thr555=
ENST00000415891.5:c.*232A>G	ENSP00000414417.1:n.*232A>G
ENST00000456385.5:c.*1332A>G	ENSP00000399029.1:n.*1332A>G
ENST00000493551.1:n.233A>G
NM_001287527.1:c.1665A>G	NP_001274456.1:p.Thr555=
NM_001287528.1:c.1665A>G	NP_001274457.1:p.Thr555=
NM_024692.5:c.1665A>G	NP_078968.3:p.Thr555=
NR_109844.1:n.1913A>G
XM_005264562.2:c.1665A>G	XP_005264619.1:p.Thr555=
XM_005264563.1:c.1665A>G	XP_005264620.1:p.Thr555=
XM_005264564.1:c.1611A>G	XP_005264621.1:p.Thr537=
XM_006712104.2:c.1665A>G	XP_006712167.1:p.Thr555=
XM_006712105.2:c.1665A>G	XP_006712168.1:p.Thr555=
XM_011533109.1:c.1665A>G	XP_011531411.1:p.Thr555=
XM_011533110.1:c.1344A>G	XP_011531412.1:p.Thr448=
XR_939717.1:n.1834A>G
XR_939718.1:n.1889A>G
XR_939719.1:n.3575A>G
XR_939720.1:n.1889A>G
XM_006712105.4:c.1665A>G	XP_006712168.1:p.Thr555=
XM_017004958.1:c.1665A>G	XP_016860447.1:p.Thr555=
XM_017004959.2:c.1665A>G	XP_016860448.1:p.Thr555=
XR_001738944.2:n.1896A>G
XR_002959339.1:n.1841A>G
XR_939717.3:n.1841A>G
XR_939718.3:n.1896A>G
XR_939719.3:n.4187A>G
NM_024692.6:c.1665A>G MANE Select	NP_078968.3:p.Thr555=
NM_001287527.2:c.1665A>G	NP_001274456.1:p.Thr555=
NM_001287528.2:c.1665A>G	NP_001274457.1:p.Thr555=
NR_109844.2:n.1724A>G