Canonical Allele Identifier: CA484516599
Gene: FARP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.99037924A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.98385670A>T , CM000675.2:g.98385670A>T GRCh38
NC_000013.10:g.99037924A>T , CM000675.1:g.99037924A>T GRCh37
NC_000013.9:g.97835925A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000319562.11:c.615A>T MANE Select ENSP00000322926.6:p.Gly205=
ENST00000596580.2:c.615A>T ENSP00000490391.1:p.Gly205=
ENST00000319562.10:c.615A>T ENSP00000322926.6:p.Gly205=
ENST00000490389.1:n.488A>T
ENST00000593548.1:n.668A>T
ENST00000595380.5:n.376A>T
ENST00000595437.5:c.615A>T ENSP00000471242.1:p.Gly205=
ENST00000596467.5:n.474A>T
ENST00000599040.5:c.-55A>T ENSP00000469420.1:n.-55A>T
ENST00000601009.1:c.217A>T
ENST00000602263.5:n.771A>T
ENST00000627049.2:c.615A>T ENSP00000486285.1:p.Gly205=
NM_001286839.1:c.615A>T NP_001273768.1:p.Gly205=
NM_005766.3:c.615A>T NP_005757.1:p.Gly205=
XM_011521046.1:c.615A>T XP_011519348.1:p.Gly205=
XM_011521046.2:c.615A>T XP_011519348.1:p.Gly205=
XM_017020312.1:c.615A>T XP_016875801.1:p.Gly205=
XM_017020313.2:c.462A>T XP_016875802.1:p.Gly154=
NM_001286839.2:c.615A>T NP_001273768.1:p.Gly205=
NM_005766.4:c.615A>T MANE Select NP_005757.1:p.Gly205=