Canonical Allele Identifier: CA2612218962

Gene: CAVIN3

Linked Data

• gnomAD v4: 11-6319602-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6319604del , CM000673.2:g.6319604del	GRCh38
NC_000011.9:g.6340834del , CM000673.1:g.6340834del	GRCh37
NC_000011.8:g.6297410del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303927.4:c.385-39del MANE Select	ENSP00000307292.3:n.385-39del
ENST00000303927.3:c.385-39del	ENSP00000307292.3:n.385-39del
ENST00000524852.1:n.132del
ENST00000530979.1:c.481-39del	ENSP00000432047.1:n.481-39del
ENST00000532354.1:n.407-39del
NM_145040.2:c.385-39del	NP_659477.2:n.385-39del
XR_242848.3:n.43del
XR_242849.3:n.43del
XR_428874.2:n.43del
XR_930992.1:n.43del
XR_930994.1:n.43del
XR_930995.1:n.43del
XR_930996.1:n.43del
XR_930997.1:n.720+1384del
XR_930998.1:n.43del
XR_930999.1:n.43del
XR_001748105.2:n.62del
XR_001748106.1:n.215del
XR_001748108.2:n.62del
XR_001748109.2:n.71del
XR_242848.4:n.464del
XR_930992.3:n.62del
XR_930994.3:n.62del
XR_930995.3:n.62del
XR_930998.3:n.62del
NM_145040.3:c.385-39del MANE Select	NP_659477.2:n.385-39del