Canonical Allele Identifier: CA388570973

Gene: FARP1

Linked Data

• MyVariant Identifiers: chr13:g.99037925C>T (hg19) ; chr13:g.98385671C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.98385671C>T , CM000675.2:g.98385671C>T	GRCh38
NC_000013.10:g.99037925C>T , CM000675.1:g.99037925C>T	GRCh37
NC_000013.9:g.97835926C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000319562.11:c.616C>T MANE Select	ENSP00000322926.6:p.Gln206Ter
ENST00000596580.2:c.616C>T	ENSP00000490391.1:p.Gln206Ter
ENST00000319562.10:c.616C>T	ENSP00000322926.6:p.Gln206Ter
ENST00000490389.1:n.489C>T
ENST00000593548.1:n.669C>T
ENST00000595380.5:n.377C>T
ENST00000595437.5:c.616C>T	ENSP00000471242.1:p.Gln206Ter
ENST00000596467.5:n.475C>T
ENST00000599040.5:c.-54C>T	ENSP00000469420.1:n.-54C>T
ENST00000601009.1:c.218C>T
ENST00000602263.5:n.772C>T
ENST00000627049.2:c.616C>T	ENSP00000486285.1:p.Gln206Ter
NM_001286839.1:c.616C>T	NP_001273768.1:p.Gln206Ter
NM_005766.3:c.616C>T	NP_005757.1:p.Gln206Ter
XM_011521046.1:c.616C>T	XP_011519348.1:p.Gln206Ter
XM_011521046.2:c.616C>T	XP_011519348.1:p.Gln206Ter
XM_017020312.1:c.616C>T	XP_016875801.1:p.Gln206Ter
XM_017020313.2:c.463C>T	XP_016875802.1:p.Gln155Ter
NM_001286839.2:c.616C>T	NP_001273768.1:p.Gln206Ter
NM_005766.4:c.616C>T MANE Select	NP_005757.1:p.Gln206Ter