Canonical Allele Identifier: CA500215489
Gene: CAVIN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.40556792C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42404774C>A , CM000679.2:g.42404774C>A GRCh38
NC_000017.10:g.40556792C>A , CM000679.1:g.40556792C>A GRCh37
NC_000017.9:g.37810318C>A NCBI36
NG_015845.1:g.23547G>T
NG_015845.2:g.23547G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000357037.6:c.1086G>T MANE Select ENSP00000349541.4:p.Arg362=
ENST00000357037.5:c.1086G>T ENSP00000349541.4:p.Arg362=
NM_012232.5:c.1086G>T NP_036364.2:p.Arg362=
NM_012232.6:c.1086G>T MANE Select NP_036364.2:p.Arg362=