Canonical Allele Identifier: CA290750300
Gene: CAVIN1 HGNC NCBI

Linked Data

dbSNP Id: rs969037683
MyVariant Identifiers: chr17:g.40556778G>T (hg19) chr17:g.42404760G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42404760G>T , CM000679.2:g.42404760G>T GRCh38
NC_000017.10:g.40556778G>T , CM000679.1:g.40556778G>T GRCh37
NC_000017.9:g.37810304G>T NCBI36
NG_015845.1:g.23561C>A
NG_015845.2:g.23561C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000357037.6:c.1100C>A MANE Select ENSP00000349541.4:p.Pro367His
ENST00000357037.5:c.1100C>A ENSP00000349541.4:p.Pro367His
NM_012232.5:c.1100C>A NP_036364.2:p.Pro367His
NM_012232.6:c.1100C>A MANE Select NP_036364.2:p.Pro367His
Search 100 bp 5'
Search 100 bp 3'