Canonical Allele Identifier: CA13836332

Gene: FARP1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.98308508C>T , CM000675.2:g.98308508C>T	GRCh38
NC_000013.10:g.98960762C>T , CM000675.1:g.98960762C>T	GRCh37
NC_000013.9:g.97758763C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319562.11:c.172-35254C>T MANE Select	ENSP00000322926.6:n.172-35254C>T
ENST00000596580.2:c.172-35254C>T	ENSP00000490391.1:n.172-35254C>T
ENST00000319562.10:c.172-35254C>T	ENSP00000322926.6:n.172-35254C>T
ENST00000595437.5:c.172-35254C>T	ENSP00000471242.1:n.172-35254C>T
ENST00000598389.5:c.172-35254C>T	ENSP00000469712.1:n.172-35254C>T
ENST00000627049.2:c.172-35254C>T	ENSP00000486285.1:n.172-35254C>T
NM_001286839.1:c.172-35254C>T	NP_001273768.1:n.172-35254C>T
NM_005766.3:c.172-35254C>T	NP_005757.1:n.172-35254C>T
XM_011521046.1:c.172-35254C>T	XP_011519348.1:n.172-35254C>T
XM_011521046.2:c.172-35254C>T	XP_011519348.1:n.172-35254C>T
XM_017020312.1:c.172-35254C>T	XP_016875801.1:n.172-35254C>T
XM_017020313.2:c.19-35254C>T	XP_016875802.1:n.19-35254C>T
NM_001286839.2:c.172-35254C>T	NP_001273768.1:n.172-35254C>T
NM_005766.4:c.172-35254C>T MANE Select	NP_005757.1:n.172-35254C>T