Canonical Allele Identifier: CA2790307724

Gene: CAVIN3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6319687G>A , CM000673.2:g.6319687G>A	GRCh38
NC_000011.9:g.6340917G>A , CM000673.1:g.6340917G>A	GRCh37
NC_000011.8:g.6297493G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303927.4:c.385-123C>T MANE Select	ENSP00000307292.3:n.385-123C>T
ENST00000303927.3:c.385-123C>T	ENSP00000307292.3:n.385-123C>T
ENST00000524852.1:n.64-16C>T
ENST00000530979.1:c.450C>T	ENSP00000432047.1:p.Ala150=
ENST00000532354.1:n.376C>T
NM_145040.2:c.385-123C>T	NP_659477.2:n.385-123C>T
XR_242848.3:n.126G>A
XR_242849.3:n.126G>A
XR_428874.2:n.126G>A
XR_930992.1:n.126G>A
XR_930994.1:n.126G>A
XR_930995.1:n.126G>A
XR_930996.1:n.126G>A
XR_930997.1:n.720+1467G>A
XR_930998.1:n.126G>A
XR_930999.1:n.126G>A
XR_001748105.2:n.145G>A
XR_001748106.1:n.298G>A
XR_001748108.2:n.145G>A
XR_001748109.2:n.154G>A
XR_242848.4:n.547G>A
XR_930992.3:n.145G>A
XR_930994.3:n.145G>A
XR_930995.3:n.145G>A
XR_930998.3:n.145G>A
NM_145040.3:c.385-123C>T MANE Select	NP_659477.2:n.385-123C>T