Canonical Allele Identifier: CA379352967

Gene: CAVIN3

Linked Data

• MyVariant Identifiers: chr11:g.6340921T>C (hg19) ; chr11:g.6319691T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6319691T>C , CM000673.2:g.6319691T>C	GRCh38
NC_000011.9:g.6340921T>C , CM000673.1:g.6340921T>C	GRCh37
NC_000011.8:g.6297497T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303927.4:c.385-127A>G MANE Select	ENSP00000307292.3:n.385-127A>G
ENST00000303927.3:c.385-127A>G	ENSP00000307292.3:n.385-127A>G
ENST00000524852.1:n.64-20A>G
ENST00000530979.1:c.446A>G	ENSP00000432047.1:p.His149Arg
ENST00000532354.1:n.372A>G
NM_145040.2:c.385-127A>G	NP_659477.2:n.385-127A>G
XR_242848.3:n.130T>C
XR_242849.3:n.130T>C
XR_428874.2:n.130T>C
XR_930992.1:n.130T>C
XR_930994.1:n.130T>C
XR_930995.1:n.130T>C
XR_930996.1:n.130T>C
XR_930997.1:n.720+1471T>C
XR_930998.1:n.130T>C
XR_930999.1:n.130T>C
XR_001748105.2:n.149T>C
XR_001748106.1:n.302T>C
XR_001748108.2:n.149T>C
XR_001748109.2:n.158T>C
XR_242848.4:n.551T>C
XR_930992.3:n.149T>C
XR_930994.3:n.149T>C
XR_930995.3:n.149T>C
XR_930998.3:n.149T>C
NM_145040.3:c.385-127A>G MANE Select	NP_659477.2:n.385-127A>G