Canonical Allele Identifier: CA388571134

Gene: FARP1

Linked Data

• dbSNP Id: rs780967752
• gnomAD v2: 13-99037968-G-T
• gnomAD v4: 13-98385714-G-T
• MyVariant Identifiers: chr13:g.99037968G>T (hg19) ; chr13:g.98385714G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.98385714G>T , CM000675.2:g.98385714G>T	GRCh38
NC_000013.10:g.99037968G>T , CM000675.1:g.99037968G>T	GRCh37
NC_000013.9:g.97835969G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319562.11:c.659G>T MANE Select	ENSP00000322926.6:p.Arg220Leu
ENST00000596580.2:c.659G>T	ENSP00000490391.1:p.Arg220Leu
ENST00000319562.10:c.659G>T	ENSP00000322926.6:p.Arg220Leu
ENST00000490389.1:n.532G>T
ENST00000593548.1:n.712G>T
ENST00000595380.5:n.420G>T
ENST00000595437.5:c.659G>T	ENSP00000471242.1:p.Arg220Leu
ENST00000596467.5:n.518G>T
ENST00000599040.5:c.-11G>T	ENSP00000469420.1:n.-11G>T
ENST00000601009.1:c.261G>T
ENST00000602263.5:n.815G>T
ENST00000627049.2:c.659G>T	ENSP00000486285.1:p.Arg220Leu
NM_001286839.1:c.659G>T	NP_001273768.1:p.Arg220Leu
NM_005766.3:c.659G>T	NP_005757.1:p.Arg220Leu
XM_011521046.1:c.659G>T	XP_011519348.1:p.Arg220Leu
XM_011521046.2:c.659G>T	XP_011519348.1:p.Arg220Leu
XM_017020312.1:c.659G>T	XP_016875801.1:p.Arg220Leu
XM_017020313.2:c.506G>T	XP_016875802.1:p.Arg169Leu
NM_001286839.2:c.659G>T	NP_001273768.1:p.Arg220Leu
NM_005766.4:c.659G>T MANE Select	NP_005757.1:p.Arg220Leu