Canonical Allele Identifier: CA217266177
Gene: CAVIN3 HGNC NCBI

Linked Data

dbSNP Id: rs954129971
gnomAD v2: 11-6340905-G-A
gnomAD v4: 11-6319675-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6319675G>A , CM000673.2:g.6319675G>A GRCh38
NC_000011.9:g.6340905G>A , CM000673.1:g.6340905G>A GRCh37
NC_000011.8:g.6297481G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303927.4:c.385-111C>T MANE Select ENSP00000307292.3:n.385-111C>T
ENST00000303927.3:c.385-111C>T ENSP00000307292.3:n.385-111C>T
ENST00000524852.1:n.64-4C>T
ENST00000530979.1:c.462C>T ENSP00000432047.1:p.Pro154=
ENST00000532354.1:n.388C>T
NM_145040.2:c.385-111C>T NP_659477.2:n.385-111C>T
XR_242848.3:n.114G>A
XR_242849.3:n.114G>A
XR_428874.2:n.114G>A
XR_930992.1:n.114G>A
XR_930994.1:n.114G>A
XR_930995.1:n.114G>A
XR_930996.1:n.114G>A
XR_930997.1:n.720+1455G>A
XR_930998.1:n.114G>A
XR_930999.1:n.114G>A
XR_001748105.2:n.133G>A
XR_001748106.1:n.286G>A
XR_001748108.2:n.133G>A
XR_001748109.2:n.142G>A
XR_242848.4:n.535G>A
XR_930992.3:n.133G>A
XR_930994.3:n.133G>A
XR_930995.3:n.133G>A
XR_930998.3:n.133G>A
NM_145040.3:c.385-111C>T MANE Select NP_659477.2:n.385-111C>T