Canonical Allele Identifier: CA500215500
Gene: CAVIN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.40556804G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42404786G>C , CM000679.2:g.42404786G>C GRCh38
NC_000017.10:g.40556804G>C , CM000679.1:g.40556804G>C GRCh37
NC_000017.9:g.37810330G>C NCBI36
NG_015845.1:g.23535C>G
NG_015845.2:g.23535C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000357037.6:c.1074C>G MANE Select ENSP00000349541.4:p.Ala358=
ENST00000357037.5:c.1074C>G ENSP00000349541.4:p.Ala358=
NM_012232.5:c.1074C>G NP_036364.2:p.Ala358=
NM_012232.6:c.1074C>G MANE Select NP_036364.2:p.Ala358=