Canonical Allele Identifier: CA255270182

Gene: FARP1

Linked Data

• dbSNP Id: rs896895778
• gnomAD v2: 13-98993945-G-A
• gnomAD v3: 13-98341691-G-A
• gnomAD v4: 13-98341691-G-A
• MyVariant Identifiers: chr13:g.98993945G>A (hg19) ; chr13:g.98341691G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.98341691G>A , CM000675.2:g.98341691G>A	GRCh38
NC_000013.10:g.98993945G>A , CM000675.1:g.98993945G>A	GRCh37
NC_000013.9:g.97791946G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319562.11:c.172-2071G>A MANE Select	ENSP00000322926.6:n.172-2071G>A
ENST00000596580.2:c.172-2071G>A	ENSP00000490391.1:n.172-2071G>A
ENST00000319562.10:c.172-2071G>A	ENSP00000322926.6:n.172-2071G>A
ENST00000595380.5:n.31-2071G>A
ENST00000595437.5:c.172-2071G>A	ENSP00000471242.1:n.172-2071G>A
ENST00000595817.5:n.352-2071G>A
ENST00000596467.5:n.31-2071G>A
ENST00000596613.5:n.532-2071G>A
ENST00000598389.5:c.172-2071G>A	ENSP00000469712.1:n.172-2071G>A
ENST00000599040.5:c.-498-2071G>A	ENSP00000469420.1:n.-498-2071G>A
ENST00000600032.5:n.383-2071G>A
ENST00000601133.5:n.381-2071G>A
ENST00000601361.1:n.407-2071G>A
ENST00000601853.5:n.31-2071G>A
ENST00000602263.5:n.327+676G>A
ENST00000627049.2:c.172-2071G>A	ENSP00000486285.1:n.172-2071G>A
NM_001286839.1:c.172-2071G>A	NP_001273768.1:n.172-2071G>A
NM_005766.3:c.172-2071G>A	NP_005757.1:n.172-2071G>A
XM_011521046.1:c.172-2071G>A	XP_011519348.1:n.172-2071G>A
XM_011521046.2:c.172-2071G>A	XP_011519348.1:n.172-2071G>A
XM_017020312.1:c.172-2071G>A	XP_016875801.1:n.172-2071G>A
XM_017020313.2:c.19-2071G>A	XP_016875802.1:n.19-2071G>A
NM_001286839.2:c.172-2071G>A	NP_001273768.1:n.172-2071G>A
NM_005766.4:c.172-2071G>A MANE Select	NP_005757.1:n.172-2071G>A