Canonical Allele Identifier: CA255270226

Gene: FARP1

Linked Data

• dbSNP Id: rs953670149
• gnomAD v2: 13-98994014-GAA-G
• gnomAD v3: 13-98341760-GAA-G
• gnomAD v4: 13-98341760-GAA-G
• MyVariant Identifiers: chr13:g.98994015_98994016del (hg19) ; chr13:g.98341761_98341762del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.98341761_98341762del , CM000675.2:g.98341761_98341762del	GRCh38
NC_000013.10:g.98994015_98994016del , CM000675.1:g.98994015_98994016del	GRCh37
NC_000013.9:g.97792016_97792017del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319562.11:c.172-2001_172-2000del MANE Select	ENSP00000322926.6:n.172-2001_172-2000del
ENST00000596580.2:c.172-2001_172-2000del	ENSP00000490391.1:n.172-2001_172-2000del
ENST00000319562.10:c.172-2001_172-2000del	ENSP00000322926.6:n.172-2001_172-2000del
ENST00000595380.5:n.31-2001_31-2000del
ENST00000595437.5:c.172-2001_172-2000del	ENSP00000471242.1:n.172-2001_172-2000del
ENST00000595817.5:n.352-2001_352-2000del
ENST00000596467.5:n.31-2001_31-2000del
ENST00000596613.5:n.532-2001_532-2000del
ENST00000598389.5:c.172-2001_172-2000del	ENSP00000469712.1:n.172-2001_172-2000del
ENST00000599040.5:c.-498-2001_-498-2000del	ENSP00000469420.1:n.-498-2001_-498-2000del
ENST00000600032.5:n.383-2001_383-2000del
ENST00000601133.5:n.381-2001_381-2000del
ENST00000601361.1:n.407-2001_407-2000del
ENST00000601853.5:n.31-2001_31-2000del
ENST00000602263.5:n.327+746_327+747del
ENST00000627049.2:c.172-2001_172-2000del	ENSP00000486285.1:n.172-2001_172-2000del
NM_001286839.1:c.172-2001_172-2000del	NP_001273768.1:n.172-2001_172-2000del
NM_005766.3:c.172-2001_172-2000del	NP_005757.1:n.172-2001_172-2000del
XM_011521046.1:c.172-2001_172-2000del	XP_011519348.1:n.172-2001_172-2000del
XM_011521046.2:c.172-2001_172-2000del	XP_011519348.1:n.172-2001_172-2000del
XM_017020312.1:c.172-2001_172-2000del	XP_016875801.1:n.172-2001_172-2000del
XM_017020313.2:c.19-2001_19-2000del	XP_016875802.1:n.19-2001_19-2000del
NM_001286839.2:c.172-2001_172-2000del	NP_001273768.1:n.172-2001_172-2000del
NM_005766.4:c.172-2001_172-2000del MANE Select	NP_005757.1:n.172-2001_172-2000del