Canonical Allele Identifier: CA379352905
Gene: CAVIN3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6319682A>G , CM000673.2:g.6319682A>G GRCh38
NC_000011.9:g.6340912A>G , CM000673.1:g.6340912A>G GRCh37
NC_000011.8:g.6297488A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303927.4:c.385-118T>C MANE Select ENSP00000307292.3:n.385-118T>C
ENST00000303927.3:c.385-118T>C ENSP00000307292.3:n.385-118T>C
ENST00000524852.1:n.64-11T>C
ENST00000530979.1:c.455T>C ENSP00000432047.1:p.Leu152Pro
ENST00000532354.1:n.381T>C
NM_145040.2:c.385-118T>C NP_659477.2:n.385-118T>C
XR_242848.3:n.121A>G
XR_242849.3:n.121A>G
XR_428874.2:n.121A>G
XR_930992.1:n.121A>G
XR_930994.1:n.121A>G
XR_930995.1:n.121A>G
XR_930996.1:n.121A>G
XR_930997.1:n.720+1462A>G
XR_930998.1:n.121A>G
XR_930999.1:n.121A>G
XR_001748105.2:n.140A>G
XR_001748106.1:n.293A>G
XR_001748108.2:n.140A>G
XR_001748109.2:n.149A>G
XR_242848.4:n.542A>G
XR_930992.3:n.140A>G
XR_930994.3:n.140A>G
XR_930995.3:n.140A>G
XR_930998.3:n.140A>G
NM_145040.3:c.385-118T>C MANE Select NP_659477.2:n.385-118T>C