Canonical Allele Identifier: CA540579000

Gene: FARP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.241357034A>T , CM000664.2:g.241357034A>T	GRCh38
NC_000002.11:g.242296449A>T , CM000664.1:g.242296449A>T	GRCh37
NC_000002.10:g.241945122A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_014808.4:c.-25+646A>T MANE Select	NP_055623.1:n.-25+646A>T
ENST00000264042.8:c.-25+646A>T MANE Select	ENSP00000264042.3:n.-25+646A>T
NM_001282983.1:c.-25+646A>T	NP_001269912.1:n.-25+646A>T
NM_001282983.2:c.-25+646A>T	NP_001269912.1:n.-25+646A>T
NM_001282984.1:c.-25+646A>T	NP_001269913.1:n.-25+646A>T
NM_001282984.2:c.-25+646A>T	NP_001269913.1:n.-25+646A>T
NM_014808.3:c.-25+646A>T	NP_055623.1:n.-25+646A>T
ENST00000264042.7:c.-25+646A>T	ENSP00000264042.3:n.-25+646A>T
ENST00000373287.8:c.-25+646A>T	ENSP00000362384.4:n.-25+646A>T
ENST00000478489.5:n.94+646A>T
ENST00000479427.5:n.90+646A>T
ENST00000627550.2:c.-25+646A>T	ENSP00000486597.1:n.-25+646A>T
XM_005247050.3:c.-25+646A>T	XP_005247107.1:n.-25+646A>T
XM_011512233.1:c.-25+646A>T	XP_011510535.1:n.-25+646A>T
XM_017005417.1:c.-387+646A>T	XP_016860906.1:n.-387+646A>T
XM_017005419.2:c.-25+646A>T	XP_016860908.1:n.-25+646A>T
XM_017005420.1:c.-25+646A>T	XP_016860909.1:n.-25+646A>T
XM_024453259.1:c.-25+679A>T	XP_024309027.1:n.-25+679A>T