Canonical Allele Identifier: CA1736911374
Gene: CAV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.116547010G= , CM000669.2:g.116547010G= GRCh38
NC_000007.13:g.116187064G= , CM000669.1:g.116187064G= GRCh37
NC_000007.12:g.115974300G= NCBI36
NG_012051.1:g.27226G=

Transcript Alleles

HGVS Amino-acid change
ENST00000341049.7:c.196-11936G= MANE Select ENSP00000339191.2:n.196-11936G=
ENST00000405348.6:c.103-11936G= ENSP00000384348.1:n.103-11936G=
ENST00000614113.5:c.*26-11936G= ENSP00000479447.2:n.*26-11936G=
ENST00000341049.6:c.196-11936G= ENSP00000339191.2:n.196-11936G=
ENST00000393467.1:c.103-11936G= ENSP00000377110.1:n.103-11936G=
ENST00000393468.1:c.103-11936G= ENSP00000377111.1:n.103-11936G=
ENST00000393470.1:c.163-11936G= ENSP00000377113.1:n.163-11936G=
ENST00000405348.5:c.103-11936G= ENSP00000384348.1:n.103-11936G=
ENST00000451122.5:c.*648-11936G= ENSP00000409541.1:n.*648-11936G=
ENST00000456473.5:c.103-11936G= ENSP00000389033.1:n.103-11936G=
ENST00000614113.4:c.103-11936G= ENSP00000479447.1:n.103-11936G=
NM_001172895.1:c.103-11936G= NP_001166366.1:n.103-11936G=
NM_001172896.1:c.103-11936G= NP_001166367.1:n.103-11936G=
NM_001172897.1:c.103-11936G= NP_001166368.1:n.103-11936G=
NM_001753.4:c.196-11936G= NP_001744.2:n.196-11936G=
NM_001753.5:c.196-11936G= MANE Select NP_001744.2:n.196-11936G=
NM_001172896.2:c.103-11936G= NP_001166367.1:n.103-11936G=
NM_001172897.2:c.103-11936G= NP_001166368.1:n.103-11936G=