Canonical Allele Identifier: CA388570960

Gene: FARP1

Linked Data

• MyVariant Identifiers: chr13:g.99037921T>G (hg19) ; chr13:g.98385667T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.98385667T>G , CM000675.2:g.98385667T>G	GRCh38
NC_000013.10:g.99037921T>G , CM000675.1:g.99037921T>G	GRCh37
NC_000013.9:g.97835922T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000319562.11:c.612T>G MANE Select	ENSP00000322926.6:p.Ile204Met
ENST00000596580.2:c.612T>G	ENSP00000490391.1:p.Ile204Met
ENST00000319562.10:c.612T>G	ENSP00000322926.6:p.Ile204Met
ENST00000490389.1:n.485T>G
ENST00000593548.1:n.665T>G
ENST00000595380.5:n.373T>G
ENST00000595437.5:c.612T>G	ENSP00000471242.1:p.Ile204Met
ENST00000596467.5:n.471T>G
ENST00000599040.5:c.-58T>G	ENSP00000469420.1:n.-58T>G
ENST00000601009.1:c.214T>G
ENST00000602263.5:n.768T>G
ENST00000627049.2:c.612T>G	ENSP00000486285.1:p.Ile204Met
NM_001286839.1:c.612T>G	NP_001273768.1:p.Ile204Met
NM_005766.3:c.612T>G	NP_005757.1:p.Ile204Met
XM_011521046.1:c.612T>G	XP_011519348.1:p.Ile204Met
XM_011521046.2:c.612T>G	XP_011519348.1:p.Ile204Met
XM_017020312.1:c.612T>G	XP_016875801.1:p.Ile204Met
XM_017020313.2:c.459T>G	XP_016875802.1:p.Ile153Met
NM_001286839.2:c.612T>G	NP_001273768.1:p.Ile204Met
NM_005766.4:c.612T>G MANE Select	NP_005757.1:p.Ile204Met