Canonical Allele Identifier: CA2581148655

Gene: FARP1

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.98443780A>C , CM000675.2:g.98443780A>C	GRCh38
NC_000013.10:g.99096034A>C , CM000675.1:g.99096034A>C	GRCh37
NC_000013.9:g.97894035A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319562.11:c.2797-2318A>C MANE Select	ENSP00000322926.6:n.2797-2318A>C
ENST00000319562.10:c.2797-2318A>C	ENSP00000322926.6:n.2797-2318A>C
ENST00000595437.5:c.2890-2318A>C	ENSP00000471242.1:n.2890-2318A>C
ENST00000627049.2:c.2890-2318A>C	ENSP00000486285.1:n.2890-2318A>C
NM_001286839.1:c.2890-2318A>C	NP_001273768.1:n.2890-2318A>C
NM_005766.3:c.2797-2318A>C	NP_005757.1:n.2797-2318A>C
XM_011521046.1:c.2890-2318A>C	XP_011519348.1:n.2890-2318A>C
XM_011521046.2:c.2890-2318A>C	XP_011519348.1:n.2890-2318A>C
XM_017020312.1:c.2797-2318A>C	XP_016875801.1:n.2797-2318A>C
XM_017020313.2:c.2737-2318A>C	XP_016875802.1:n.2737-2318A>C
NM_001286839.2:c.2890-2318A>C	NP_001273768.1:n.2890-2318A>C
NM_005766.4:c.2797-2318A>C MANE Select	NP_005757.1:n.2797-2318A>C