Canonical Allele Identifier: CA2728625502
Gene: FARP1 HGNC NCBI

Linked Data

dbSNP Id: rs1887985176

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.98341805T>C , CM000675.2:g.98341805T>C GRCh38
NC_000013.10:g.98994059T>C , CM000675.1:g.98994059T>C GRCh37
NC_000013.9:g.97792060T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000319562.11:c.172-1957T>C MANE Select ENSP00000322926.6:n.172-1957T>C
ENST00000596580.2:c.172-1957T>C ENSP00000490391.1:n.172-1957T>C
ENST00000319562.10:c.172-1957T>C ENSP00000322926.6:n.172-1957T>C
ENST00000595380.5:n.31-1957T>C
ENST00000595437.5:c.172-1957T>C ENSP00000471242.1:n.172-1957T>C
ENST00000595817.5:n.352-1957T>C
ENST00000596467.5:n.31-1957T>C
ENST00000596613.5:n.532-1957T>C
ENST00000598389.5:c.172-1957T>C ENSP00000469712.1:n.172-1957T>C
ENST00000599040.5:c.-498-1957T>C ENSP00000469420.1:n.-498-1957T>C
ENST00000600032.5:n.383-1957T>C
ENST00000601133.5:n.381-1957T>C
ENST00000601361.1:n.407-1957T>C
ENST00000601853.5:n.31-1957T>C
ENST00000602263.5:n.327+790T>C
ENST00000627049.2:c.172-1957T>C ENSP00000486285.1:n.172-1957T>C
NM_001286839.1:c.172-1957T>C NP_001273768.1:n.172-1957T>C
NM_005766.3:c.172-1957T>C NP_005757.1:n.172-1957T>C
XM_011521046.1:c.172-1957T>C XP_011519348.1:n.172-1957T>C
XM_011521046.2:c.172-1957T>C XP_011519348.1:n.172-1957T>C
XM_017020312.1:c.172-1957T>C XP_016875801.1:n.172-1957T>C
XM_017020313.2:c.19-1957T>C XP_016875802.1:n.19-1957T>C
NM_001286839.2:c.172-1957T>C NP_001273768.1:n.172-1957T>C
NM_005766.4:c.172-1957T>C MANE Select NP_005757.1:n.172-1957T>C