Canonical Allele Identifier: CA217266142
Gene: CAVIN3 HGNC NCBI

Linked Data

dbSNP Id: rs998468387
gnomAD v2: 11-6340878-A-G
gnomAD v3: 11-6319648-A-G
gnomAD v4: 11-6319648-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6319648A>G , CM000673.2:g.6319648A>G GRCh38
NC_000011.9:g.6340878A>G , CM000673.1:g.6340878A>G GRCh37
NC_000011.8:g.6297454A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303927.4:c.385-84T>C MANE Select ENSP00000307292.3:n.385-84T>C
ENST00000303927.3:c.385-84T>C ENSP00000307292.3:n.385-84T>C
ENST00000524852.1:n.87T>C
ENST00000530979.1:c.480+9T>C ENSP00000432047.1:n.480+9T>C
ENST00000532354.1:n.406+9T>C
NM_145040.2:c.385-84T>C NP_659477.2:n.385-84T>C
XR_242848.3:n.87A>G
XR_242849.3:n.87A>G
XR_428874.2:n.87A>G
XR_930992.1:n.87A>G
XR_930994.1:n.87A>G
XR_930995.1:n.87A>G
XR_930996.1:n.87A>G
XR_930997.1:n.720+1428A>G
XR_930998.1:n.87A>G
XR_930999.1:n.87A>G
XR_001748105.2:n.106A>G
XR_001748106.1:n.259A>G
XR_001748108.2:n.106A>G
XR_001748109.2:n.115A>G
XR_242848.4:n.508A>G
XR_930992.3:n.106A>G
XR_930994.3:n.106A>G
XR_930995.3:n.106A>G
XR_930998.3:n.106A>G
NM_145040.3:c.385-84T>C MANE Select NP_659477.2:n.385-84T>C