Canonical Allele Identifier: CA3400586

Gene: FNIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.131672501T>C , CM000667.2:g.131672501T>C	GRCh38
NC_000005.9:g.131008194T>C , CM000667.1:g.131008194T>C	GRCh37
NC_000005.8:g.131036093T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510461.6:c.1943A>G MANE Select	ENSP00000421985.1:p.Gln648Arg
ENST00000307954.12:c.1808A>G	ENSP00000310453.8:p.Gln603Arg
ENST00000307968.11:c.1859A>G	ENSP00000309266.7:p.Gln620Arg
ENST00000510461.5:c.1943A>G	ENSP00000421985.1:p.Gln648Arg
ENST00000514667.1:c.220-67808A>G	ENSP00000426948.1:n.220-67808A>G
ENST00000615660.4:c.1199A>G	ENSP00000480650.1:p.Gln400Arg
NM_001008738.2:c.1859A>G	NP_001008738.2:p.Gln620Arg
NM_133372.2:c.1943A>G	NP_588613.2:p.Gln648Arg
NM_001346114.1:c.1808A>G	NP_001333043.1:p.Gln603Arg
NM_133372.3:c.1943A>G MANE Select	NP_588613.3:p.Gln648Arg
NM_001008738.3:c.1859A>G	NP_001008738.3:p.Gln620Arg
NM_001346114.2:c.1808A>G	NP_001333043.1:p.Gln603Arg