Canonical Allele Identifier: CA379352418
Gene: CAVIN3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.6340701C>G (hg19) chr11:g.6319471C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6319471C>G , CM000673.2:g.6319471C>G GRCh38
NC_000011.9:g.6340701C>G , CM000673.1:g.6340701C>G GRCh37
NC_000011.8:g.6297277C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303927.4:c.478G>C MANE Select ENSP00000307292.3:p.Ala160Pro
ENST00000303927.3:c.478G>C ENSP00000307292.3:p.Ala160Pro
ENST00000524852.1:n.264G>C
ENST00000530979.1:c.574G>C ENSP00000432047.1:p.Ala192Pro
ENST00000532354.1:n.500G>C
NM_145040.2:c.478G>C NP_659477.2:p.Ala160Pro
XR_930997.1:n.720+1251C>G
XR_001748106.1:n.82C>G
XR_242848.4:n.331C>G
NM_145040.3:c.478G>C MANE Select NP_659477.2:p.Ala160Pro
Search 100 bp 5'
Search 100 bp 3'