Canonical Allele Identifier: CA500215514
Gene: CAVIN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.40556825G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42404807G>T , CM000679.2:g.42404807G>T GRCh38
NC_000017.10:g.40556825G>T , CM000679.1:g.40556825G>T GRCh37
NC_000017.9:g.37810351G>T NCBI36
NG_015845.1:g.23514C>A
NG_015845.2:g.23514C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000357037.6:c.1053C>A MANE Select ENSP00000349541.4:p.Gly351=
ENST00000357037.5:c.1053C>A ENSP00000349541.4:p.Gly351=
NM_012232.5:c.1053C>A NP_036364.2:p.Gly351=
NM_012232.6:c.1053C>A MANE Select NP_036364.2:p.Gly351=