Canonical Allele Identifier: CA217266228

Gene: CAVIN3

Linked Data

• dbSNP Id: rs555764326
• gnomAD v2: 11-6341036-C-T
• gnomAD v3: 11-6319806-C-T
• gnomAD v4: 11-6319806-C-T
• MyVariant Identifiers: chr11:g.6341036C>T (hg19) ; chr11:g.6319806C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6319806C>T , CM000673.2:g.6319806C>T	GRCh38
NC_000011.9:g.6341036C>T , CM000673.1:g.6341036C>T	GRCh37
NC_000011.8:g.6297612C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303927.4:c.385-242G>A MANE Select	ENSP00000307292.3:n.385-242G>A
ENST00000303927.3:c.385-242G>A	ENSP00000307292.3:n.385-242G>A
ENST00000524852.1:n.64-135G>A
ENST00000530979.1:c.385-54G>A	ENSP00000432047.1:n.385-54G>A
ENST00000532354.1:n.257G>A
NM_145040.2:c.385-242G>A	NP_659477.2:n.385-242G>A
XR_242848.3:n.136+109C>T
XR_242849.3:n.136+109C>T
XR_428874.2:n.136+109C>T
XR_930992.1:n.136+109C>T
XR_930994.1:n.136+109C>T
XR_930995.1:n.136+109C>T
XR_930996.1:n.136+109C>T
XR_930997.1:n.720+1586C>T
XR_930998.1:n.136+109C>T
XR_930999.1:n.136+109C>T
XR_001748105.2:n.155+109C>T
XR_001748106.1:n.308+109C>T
XR_001748108.2:n.155+109C>T
XR_001748109.2:n.164+109C>T
XR_242848.4:n.557+109C>T
XR_930992.3:n.155+109C>T
XR_930994.3:n.155+109C>T
XR_930995.3:n.155+109C>T
XR_930998.3:n.155+109C>T
NM_145040.3:c.385-242G>A MANE Select	NP_659477.2:n.385-242G>A