Canonical Allele Identifier: CA2728625492

Gene: FARP1

Linked Data

• dbSNP Id: rs1887982780

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.98341727G>T , CM000675.2:g.98341727G>T	GRCh38
NC_000013.10:g.98993981G>T , CM000675.1:g.98993981G>T	GRCh37
NC_000013.9:g.97791982G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319562.11:c.172-2035G>T MANE Select	ENSP00000322926.6:n.172-2035G>T
ENST00000596580.2:c.172-2035G>T	ENSP00000490391.1:n.172-2035G>T
ENST00000319562.10:c.172-2035G>T	ENSP00000322926.6:n.172-2035G>T
ENST00000595380.5:n.31-2035G>T
ENST00000595437.5:c.172-2035G>T	ENSP00000471242.1:n.172-2035G>T
ENST00000595817.5:n.352-2035G>T
ENST00000596467.5:n.31-2035G>T
ENST00000596613.5:n.532-2035G>T
ENST00000598389.5:c.172-2035G>T	ENSP00000469712.1:n.172-2035G>T
ENST00000599040.5:c.-498-2035G>T	ENSP00000469420.1:n.-498-2035G>T
ENST00000600032.5:n.383-2035G>T
ENST00000601133.5:n.381-2035G>T
ENST00000601361.1:n.407-2035G>T
ENST00000601853.5:n.31-2035G>T
ENST00000602263.5:n.327+712G>T
ENST00000627049.2:c.172-2035G>T	ENSP00000486285.1:n.172-2035G>T
NM_001286839.1:c.172-2035G>T	NP_001273768.1:n.172-2035G>T
NM_005766.3:c.172-2035G>T	NP_005757.1:n.172-2035G>T
XM_011521046.1:c.172-2035G>T	XP_011519348.1:n.172-2035G>T
XM_011521046.2:c.172-2035G>T	XP_011519348.1:n.172-2035G>T
XM_017020312.1:c.172-2035G>T	XP_016875801.1:n.172-2035G>T
XM_017020313.2:c.19-2035G>T	XP_016875802.1:n.19-2035G>T
NM_001286839.2:c.172-2035G>T	NP_001273768.1:n.172-2035G>T
NM_005766.4:c.172-2035G>T MANE Select	NP_005757.1:n.172-2035G>T