Canonical Allele Identifier: CA360788668

Gene: FNIP1

Linked Data

• MyVariant Identifiers: chr5:g.131007485A>C (hg19) ; chr5:g.131671792A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.131671792A>C , CM000667.2:g.131671792A>C	GRCh38
NC_000005.9:g.131007485A>C , CM000667.1:g.131007485A>C	GRCh37
NC_000005.8:g.131035384A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510461.6:c.2652T>G MANE Select	ENSP00000421985.1:p.Phe884Leu
ENST00000307954.12:c.2517T>G	ENSP00000310453.8:p.Phe839Leu
ENST00000307968.11:c.2568T>G	ENSP00000309266.7:p.Phe856Leu
ENST00000510461.5:c.2652T>G	ENSP00000421985.1:p.Phe884Leu
ENST00000514667.1:c.220-67099T>G	ENSP00000426948.1:n.220-67099T>G
ENST00000615660.4:c.1908T>G	ENSP00000480650.1:p.Phe636Leu
NM_001008738.2:c.2568T>G	NP_001008738.2:p.Phe856Leu
NM_133372.2:c.2652T>G	NP_588613.2:p.Phe884Leu
NM_001346114.1:c.2517T>G	NP_001333043.1:p.Phe839Leu
NM_133372.3:c.2652T>G MANE Select	NP_588613.3:p.Phe884Leu
NM_001008738.3:c.2568T>G	NP_001008738.3:p.Phe856Leu
NM_001346114.2:c.2517T>G	NP_001333043.1:p.Phe839Leu