Canonical Allele Identifier: CA388570980

Gene: FARP1

Linked Data

• MyVariant Identifiers: chr13:g.99037926A>G (hg19) ; chr13:g.98385672A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.98385672A>G , CM000675.2:g.98385672A>G	GRCh38
NC_000013.10:g.99037926A>G , CM000675.1:g.99037926A>G	GRCh37
NC_000013.9:g.97835927A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000319562.11:c.617A>G MANE Select	ENSP00000322926.6:p.Gln206Arg
ENST00000596580.2:c.617A>G	ENSP00000490391.1:p.Gln206Arg
ENST00000319562.10:c.617A>G	ENSP00000322926.6:p.Gln206Arg
ENST00000490389.1:n.490A>G
ENST00000593548.1:n.670A>G
ENST00000595380.5:n.378A>G
ENST00000595437.5:c.617A>G	ENSP00000471242.1:p.Gln206Arg
ENST00000596467.5:n.476A>G
ENST00000599040.5:c.-53A>G	ENSP00000469420.1:n.-53A>G
ENST00000601009.1:c.219A>G
ENST00000602263.5:n.773A>G
ENST00000627049.2:c.617A>G	ENSP00000486285.1:p.Gln206Arg
NM_001286839.1:c.617A>G	NP_001273768.1:p.Gln206Arg
NM_005766.3:c.617A>G	NP_005757.1:p.Gln206Arg
XM_011521046.1:c.617A>G	XP_011519348.1:p.Gln206Arg
XM_011521046.2:c.617A>G	XP_011519348.1:p.Gln206Arg
XM_017020312.1:c.617A>G	XP_016875801.1:p.Gln206Arg
XM_017020313.2:c.464A>G	XP_016875802.1:p.Gln155Arg
NM_001286839.2:c.617A>G	NP_001273768.1:p.Gln206Arg
NM_005766.4:c.617A>G MANE Select	NP_005757.1:p.Gln206Arg