Canonical Allele Identifier: CA1736913161
Gene: CAV2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.116508234T= , CM000669.2:g.116508234T= GRCh38
NC_000007.13:g.116148288T= , CM000669.1:g.116148288T= GRCh37
NC_000007.12:g.115935524T= NCBI36
NG_029920.1:g.13634T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000222693.5:c.*2113T= MANE Select ENSP00000222693.4:n.*2113T=
ENST00000222693.4:c.*2113T= ENSP00000222693.4:n.*2113T=
NM_001206747.1:c.*2113T= NP_001193676.1:n.*2113T=
NM_001206748.1:c.*2113T= NP_001193677.1:n.*2113T=
NM_001233.4:c.*2113T= NP_001224.1:n.*2113T=
NM_198212.2:c.*2075T= NP_937855.1:n.*2075T=
NM_001233.5:c.*2113T= MANE Select NP_001224.1:n.*2113T=
NM_001206747.2:c.*2113T= NP_001193676.1:n.*2113T=
NM_001206748.2:c.*2113T= NP_001193677.1:n.*2113T=
NM_198212.3:c.*2075T= NP_937855.1:n.*2075T=