Canonical Allele Identifier: CA500215472
Gene: CAVIN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.40556765C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42404747C>T , CM000679.2:g.42404747C>T GRCh38
NC_000017.10:g.40556765C>T , CM000679.1:g.40556765C>T GRCh37
NC_000017.9:g.37810291C>T NCBI36
NG_015845.1:g.23574G>A
NG_015845.2:g.23574G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000357037.6:c.1113G>A MANE Select ENSP00000349541.4:p.Ala371=
ENST00000357037.5:c.1113G>A ENSP00000349541.4:p.Ala371=
NM_012232.5:c.1113G>A NP_036364.2:p.Ala371=
NM_012232.6:c.1113G>A MANE Select NP_036364.2:p.Ala371=