Canonical Allele Identifier: CA484516602

Gene: FARP1

Linked Data

• MyVariant Identifiers: chr13:g.99037930A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.98385676A>T , CM000675.2:g.98385676A>T	GRCh38
NC_000013.10:g.99037930A>T , CM000675.1:g.99037930A>T	GRCh37
NC_000013.9:g.97835931A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000319562.11:c.621A>T MANE Select	ENSP00000322926.6:p.Thr207=
ENST00000596580.2:c.621A>T	ENSP00000490391.1:p.Thr207=
ENST00000319562.10:c.621A>T	ENSP00000322926.6:p.Thr207=
ENST00000490389.1:n.494A>T
ENST00000593548.1:n.674A>T
ENST00000595380.5:n.382A>T
ENST00000595437.5:c.621A>T	ENSP00000471242.1:p.Thr207=
ENST00000596467.5:n.480A>T
ENST00000599040.5:c.-49A>T	ENSP00000469420.1:n.-49A>T
ENST00000601009.1:c.223A>T
ENST00000602263.5:n.777A>T
ENST00000627049.2:c.621A>T	ENSP00000486285.1:p.Thr207=
NM_001286839.1:c.621A>T	NP_001273768.1:p.Thr207=
NM_005766.3:c.621A>T	NP_005757.1:p.Thr207=
XM_011521046.1:c.621A>T	XP_011519348.1:p.Thr207=
XM_011521046.2:c.621A>T	XP_011519348.1:p.Thr207=
XM_017020312.1:c.621A>T	XP_016875801.1:p.Thr207=
XM_017020313.2:c.468A>T	XP_016875802.1:p.Thr156=
NM_001286839.2:c.621A>T	NP_001273768.1:p.Thr207=
NM_005766.4:c.621A>T MANE Select	NP_005757.1:p.Thr207=