Canonical Allele Identifier: CA500215505
Gene: CAVIN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.40556813G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42404795G>C , CM000679.2:g.42404795G>C GRCh38
NC_000017.10:g.40556813G>C , CM000679.1:g.40556813G>C GRCh37
NC_000017.9:g.37810339G>C NCBI36
NG_015845.1:g.23526C>G
NG_015845.2:g.23526C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000357037.6:c.1065C>G MANE Select ENSP00000349541.4:p.Arg355=
ENST00000357037.5:c.1065C>G ENSP00000349541.4:p.Arg355=
NM_012232.5:c.1065C>G NP_036364.2:p.Arg355=
NM_012232.6:c.1065C>G MANE Select NP_036364.2:p.Arg355=