Canonical Allele Identifier: CA399582729
Gene: CAVIN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.40556845C>T (hg19) chr17:g.42404827C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42404827C>T , CM000679.2:g.42404827C>T GRCh38
NC_000017.10:g.40556845C>T , CM000679.1:g.40556845C>T GRCh37
NC_000017.9:g.37810371C>T NCBI36
NG_015845.1:g.23494G>A
NG_015845.2:g.23494G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000357037.6:c.1033G>A MANE Select ENSP00000349541.4:p.Gly345Ser
ENST00000357037.5:c.1033G>A ENSP00000349541.4:p.Gly345Ser
NM_012232.5:c.1033G>A NP_036364.2:p.Gly345Ser
NM_012232.6:c.1033G>A MANE Select NP_036364.2:p.Gly345Ser
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Search 100 bp 3'