Canonical Allele Identifier: CA500215452
Gene: CAVIN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.40556735G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42404717G>T , CM000679.2:g.42404717G>T GRCh38
NC_000017.10:g.40556735G>T , CM000679.1:g.40556735G>T GRCh37
NC_000017.9:g.37810261G>T NCBI36
NG_015845.1:g.23604C>A
NG_015845.2:g.23604C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000357037.6:c.1143C>A MANE Select ENSP00000349541.4:p.Ala381=
ENST00000357037.5:c.1143C>A ENSP00000349541.4:p.Ala381=
NM_012232.5:c.1143C>A NP_036364.2:p.Ala381=
NM_012232.6:c.1143C>A MANE Select NP_036364.2:p.Ala381=