Canonical Allele Identifier: CA388570985

Gene: FARP1

Linked Data

• MyVariant Identifiers: chr13:g.99037928A>C (hg19) ; chr13:g.98385674A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.98385674A>C , CM000675.2:g.98385674A>C	GRCh38
NC_000013.10:g.99037928A>C , CM000675.1:g.99037928A>C	GRCh37
NC_000013.9:g.97835929A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000319562.11:c.619A>C MANE Select	ENSP00000322926.6:p.Thr207Pro
ENST00000596580.2:c.619A>C	ENSP00000490391.1:p.Thr207Pro
ENST00000319562.10:c.619A>C	ENSP00000322926.6:p.Thr207Pro
ENST00000490389.1:n.492A>C
ENST00000593548.1:n.672A>C
ENST00000595380.5:n.380A>C
ENST00000595437.5:c.619A>C	ENSP00000471242.1:p.Thr207Pro
ENST00000596467.5:n.478A>C
ENST00000599040.5:c.-51A>C	ENSP00000469420.1:n.-51A>C
ENST00000601009.1:c.221A>C
ENST00000602263.5:n.775A>C
ENST00000627049.2:c.619A>C	ENSP00000486285.1:p.Thr207Pro
NM_001286839.1:c.619A>C	NP_001273768.1:p.Thr207Pro
NM_005766.3:c.619A>C	NP_005757.1:p.Thr207Pro
XM_011521046.1:c.619A>C	XP_011519348.1:p.Thr207Pro
XM_011521046.2:c.619A>C	XP_011519348.1:p.Thr207Pro
XM_017020312.1:c.619A>C	XP_016875801.1:p.Thr207Pro
XM_017020313.2:c.466A>C	XP_016875802.1:p.Thr156Pro
NM_001286839.2:c.619A>C	NP_001273768.1:p.Thr207Pro
NM_005766.4:c.619A>C MANE Select	NP_005757.1:p.Thr207Pro