Canonical Allele Identifier: CA255270172

Gene: FARP1

Linked Data

• dbSNP Id: rs896085316
• gnomAD v2: 13-98993928-CTG-C
• gnomAD v3: 13-98341674-CTG-C
• gnomAD v4: 13-98341674-CTG-C
• MyVariant Identifiers: chr13:g.98993929_98993930del (hg19) ; chr13:g.98341675_98341676del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.98341677_98341678del , CM000675.2:g.98341677_98341678del	GRCh38
NC_000013.10:g.98993931_98993932del , CM000675.1:g.98993931_98993932del	GRCh37
NC_000013.9:g.97791932_97791933del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319562.11:c.172-2085_172-2084del MANE Select	ENSP00000322926.6:n.172-2085_172-2084del
ENST00000596580.2:c.172-2085_172-2084del	ENSP00000490391.1:n.172-2085_172-2084del
ENST00000319562.10:c.172-2085_172-2084del	ENSP00000322926.6:n.172-2085_172-2084del
ENST00000595380.5:n.31-2085_31-2084del
ENST00000595437.5:c.172-2085_172-2084del	ENSP00000471242.1:n.172-2085_172-2084del
ENST00000595817.5:n.352-2085_352-2084del
ENST00000596467.5:n.31-2085_31-2084del
ENST00000596613.5:n.532-2085_532-2084del
ENST00000598389.5:c.172-2085_172-2084del	ENSP00000469712.1:n.172-2085_172-2084del
ENST00000599040.5:c.-498-2085_-498-2084del	ENSP00000469420.1:n.-498-2085_-498-2084del
ENST00000600032.5:n.383-2085_383-2084del
ENST00000601133.5:n.381-2085_381-2084del
ENST00000601361.1:n.407-2085_407-2084del
ENST00000601853.5:n.31-2085_31-2084del
ENST00000602263.5:n.327+662_327+663del
ENST00000627049.2:c.172-2085_172-2084del	ENSP00000486285.1:n.172-2085_172-2084del
NM_001286839.1:c.172-2085_172-2084del	NP_001273768.1:n.172-2085_172-2084del
NM_005766.3:c.172-2085_172-2084del	NP_005757.1:n.172-2085_172-2084del
XM_011521046.1:c.172-2085_172-2084del	XP_011519348.1:n.172-2085_172-2084del
XM_011521046.2:c.172-2085_172-2084del	XP_011519348.1:n.172-2085_172-2084del
XM_017020312.1:c.172-2085_172-2084del	XP_016875801.1:n.172-2085_172-2084del
XM_017020313.2:c.19-2085_19-2084del	XP_016875802.1:n.19-2085_19-2084del
NM_001286839.2:c.172-2085_172-2084del	NP_001273768.1:n.172-2085_172-2084del
NM_005766.4:c.172-2085_172-2084del MANE Select	NP_005757.1:n.172-2085_172-2084del