Canonical Allele Identifier: CA13912560

Gene: FARP1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.98174781G>C , CM000675.2:g.98174781G>C	GRCh38
NC_000013.10:g.98827035G>C , CM000675.1:g.98827035G>C	GRCh37
NC_000013.9:g.97625036G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319562.11:c.-24+31289G>C MANE Select	ENSP00000322926.6:n.-24+31289G>C
ENST00000596580.2:c.-24+31289G>C	ENSP00000490391.1:n.-24+31289G>C
ENST00000319562.10:c.-24+31289G>C	ENSP00000322926.6:n.-24+31289G>C
ENST00000376581.9:c.-24+31289G>C	ENSP00000365765.4:n.-24+31289G>C
ENST00000595437.5:c.-24+32004G>C	ENSP00000471242.1:n.-24+32004G>C
ENST00000600648.1:n.420+15183G>C
ENST00000627049.2:c.-24+31289G>C	ENSP00000486285.1:n.-24+31289G>C
NM_001001715.3:c.-24+31289G>C	NP_001001715.2:n.-24+31289G>C
NM_001286839.1:c.-24+32004G>C	NP_001273768.1:n.-24+32004G>C
NM_005766.3:c.-24+31289G>C	NP_005757.1:n.-24+31289G>C
XM_011521046.1:c.-24+31289G>C	XP_011519348.1:n.-24+31289G>C
XM_011521046.2:c.-24+31289G>C	XP_011519348.1:n.-24+31289G>C
XM_017020312.1:c.-24+32004G>C	XP_016875801.1:n.-24+32004G>C
NM_001001715.4:c.-24+31289G>C	NP_001001715.2:n.-24+31289G>C
NM_001286839.2:c.-24+32004G>C	NP_001273768.1:n.-24+32004G>C
NM_005766.4:c.-24+31289G>C MANE Select	NP_005757.1:n.-24+31289G>C