Canonical Allele Identifier: CA360788289

Gene: FNIP1

Linked Data

• MyVariant Identifiers: chr5:g.131007425G>T (hg19) ; chr5:g.131671732G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.131671732G>T , CM000667.2:g.131671732G>T	GRCh38
NC_000005.9:g.131007425G>T , CM000667.1:g.131007425G>T	GRCh37
NC_000005.8:g.131035324G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510461.6:c.2712C>A MANE Select	ENSP00000421985.1:p.Asp904Glu
ENST00000307954.12:c.2577C>A	ENSP00000310453.8:p.Asp859Glu
ENST00000307968.11:c.2628C>A	ENSP00000309266.7:p.Asp876Glu
ENST00000510461.5:c.2712C>A	ENSP00000421985.1:p.Asp904Glu
ENST00000514667.1:c.220-67039C>A	ENSP00000426948.1:n.220-67039C>A
ENST00000615660.4:c.1968C>A	ENSP00000480650.1:p.Asp656Glu
NM_001008738.2:c.2628C>A	NP_001008738.2:p.Asp876Glu
NM_133372.2:c.2712C>A	NP_588613.2:p.Asp904Glu
NM_001346114.1:c.2577C>A	NP_001333043.1:p.Asp859Glu
NM_133372.3:c.2712C>A MANE Select	NP_588613.3:p.Asp904Glu
NM_001008738.3:c.2628C>A	NP_001008738.3:p.Asp876Glu
NM_001346114.2:c.2577C>A	NP_001333043.1:p.Asp859Glu