Canonical Allele Identifier: CA2612218923
Gene: CAVIN3 HGNC NCBI

Linked Data

gnomAD v4: 11-6319577-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6319577G>A , CM000673.2:g.6319577G>A GRCh38
NC_000011.9:g.6340807G>A , CM000673.1:g.6340807G>A GRCh37
NC_000011.8:g.6297383G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303927.4:c.385-13C>T MANE Select ENSP00000307292.3:n.385-13C>T
ENST00000303927.3:c.385-13C>T ENSP00000307292.3:n.385-13C>T
ENST00000524852.1:n.158C>T
ENST00000530979.1:c.481-13C>T ENSP00000432047.1:n.481-13C>T
ENST00000532354.1:n.407-13C>T
NM_145040.2:c.385-13C>T NP_659477.2:n.385-13C>T
XR_242848.3:n.16G>A
XR_242849.3:n.16G>A
XR_428874.2:n.16G>A
XR_930992.1:n.16G>A
XR_930994.1:n.16G>A
XR_930995.1:n.16G>A
XR_930996.1:n.16G>A
XR_930997.1:n.720+1357G>A
XR_930998.1:n.16G>A
XR_930999.1:n.16G>A
XR_001748105.2:n.35G>A
XR_001748106.1:n.188G>A
XR_001748108.2:n.35G>A
XR_001748109.2:n.44G>A
XR_242848.4:n.437G>A
XR_930992.3:n.35G>A
XR_930994.3:n.35G>A
XR_930995.3:n.35G>A
XR_930998.3:n.35G>A
NM_145040.3:c.385-13C>T MANE Select NP_659477.2:n.385-13C>T