Canonical Allele Identifier: CA702915481

Gene: FARP1

Linked Data

• dbSNP Id: rs1363048626
• MyVariant Identifiers: chr13:g.98994087T>C (hg19) ; chr13:g.98341833T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.98341833T>C , CM000675.2:g.98341833T>C	GRCh38
NC_000013.10:g.98994087T>C , CM000675.1:g.98994087T>C	GRCh37
NC_000013.9:g.97792088T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000319562.11:c.172-1929T>C MANE Select	ENSP00000322926.6:n.172-1929T>C
ENST00000596580.2:c.172-1929T>C	ENSP00000490391.1:n.172-1929T>C
ENST00000319562.10:c.172-1929T>C	ENSP00000322926.6:n.172-1929T>C
ENST00000595380.5:n.31-1929T>C
ENST00000595437.5:c.172-1929T>C	ENSP00000471242.1:n.172-1929T>C
ENST00000595817.5:n.352-1929T>C
ENST00000596467.5:n.31-1929T>C
ENST00000596613.5:n.532-1929T>C
ENST00000598389.5:c.172-1929T>C	ENSP00000469712.1:n.172-1929T>C
ENST00000599040.5:c.-498-1929T>C	ENSP00000469420.1:n.-498-1929T>C
ENST00000600032.5:n.383-1929T>C
ENST00000601133.5:n.381-1929T>C
ENST00000601361.1:n.407-1929T>C
ENST00000601853.5:n.31-1929T>C
ENST00000602263.5:n.327+818T>C
ENST00000627049.2:c.172-1929T>C	ENSP00000486285.1:n.172-1929T>C
NM_001286839.1:c.172-1929T>C	NP_001273768.1:n.172-1929T>C
NM_005766.3:c.172-1929T>C	NP_005757.1:n.172-1929T>C
XM_011521046.1:c.172-1929T>C	XP_011519348.1:n.172-1929T>C
XM_011521046.2:c.172-1929T>C	XP_011519348.1:n.172-1929T>C
XM_017020312.1:c.172-1929T>C	XP_016875801.1:n.172-1929T>C
XM_017020313.2:c.19-1929T>C	XP_016875802.1:n.19-1929T>C
NM_001286839.2:c.172-1929T>C	NP_001273768.1:n.172-1929T>C
NM_005766.4:c.172-1929T>C MANE Select	NP_005757.1:n.172-1929T>C