Canonical Allele Identifier: CA388570954

Gene: FARP1

Linked Data

• MyVariant Identifiers: chr13:g.99037920G>A (hg19) ; chr13:g.98385666G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.98385666G>A , CM000675.2:g.98385666G>A	GRCh38
NC_000013.10:g.99037920G>A , CM000675.1:g.99037920G>A	GRCh37
NC_000013.9:g.97835921G>A	NCBI36

Transcript Alleles

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