Canonical Allele Identifier: CA1950112755

Gene: CAVIN3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6319606C= , CM000673.2:g.6319606C=	GRCh38
NC_000011.9:g.6340836C= , CM000673.1:g.6340836C=	GRCh37
NC_000011.8:g.6297412C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303927.4:c.385-42G= MANE Select	ENSP00000307292.3:n.385-42G=
ENST00000303927.3:c.385-42G=	ENSP00000307292.3:n.385-42G=
ENST00000524852.1:n.129G=
ENST00000530979.1:c.481-42G=	ENSP00000432047.1:n.481-42G=
ENST00000532354.1:n.407-42G=
NM_145040.2:c.385-42G=	NP_659477.2:n.385-42G=
XR_242848.3:n.45C=
XR_242849.3:n.45C=
XR_428874.2:n.45C=
XR_930992.1:n.45C=
XR_930994.1:n.45C=
XR_930995.1:n.45C=
XR_930996.1:n.45C=
XR_930997.1:n.720+1386C=
XR_930998.1:n.45C=
XR_930999.1:n.45C=
XR_001748105.2:n.64C=
XR_001748106.1:n.217C=
XR_001748108.2:n.64C=
XR_001748109.2:n.73C=
XR_242848.4:n.466C=
XR_930992.3:n.64C=
XR_930994.3:n.64C=
XR_930995.3:n.64C=
XR_930998.3:n.64C=
NM_145040.3:c.385-42G= MANE Select	NP_659477.2:n.385-42G=