Canonical Allele Identifier: CA1339610390

Gene: FARP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.241431686C= , CM000664.2:g.241431686C=	GRCh38
NC_000002.11:g.242371101C= , CM000664.1:g.242371101C=	GRCh37
NC_000002.10:g.242019774C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_014808.4:c.779C= MANE Select	NP_055623.1:p.Thr260=
ENST00000264042.8:c.779C= MANE Select	ENSP00000264042.3:p.Thr260=
NM_001282983.1:c.779C=	NP_001269912.1:p.Thr260=
NM_001282983.2:c.779C=	NP_001269912.1:p.Thr260=
NM_001282984.1:c.779C=	NP_001269913.1:p.Thr260=
NM_001282984.2:c.779C=	NP_001269913.1:p.Thr260=
NM_014808.3:c.779C=	NP_055623.1:p.Thr260=
ENST00000264042.7:c.779C=	ENSP00000264042.3:p.Thr260=
ENST00000373287.8:c.779C=	ENSP00000362384.4:p.Thr260=
ENST00000471447.5:n.461C=
ENST00000485051.1:n.457C=
ENST00000627550.2:c.779C=	ENSP00000486597.1:p.Thr260=
XM_005247050.3:c.779C=	XP_005247107.1:p.Thr260=
XM_011512233.1:c.779C=	XP_011510535.1:p.Thr260=
XM_011512234.1:c.779C=	XP_011510536.1:p.Thr260=
XM_011512235.1:c.632C=	XP_011510537.1:p.Thr211=
XM_011512236.1:c.521C=	XP_011510538.1:p.Thr174=
XM_011512237.1:c.521C=	XP_011510539.1:p.Thr174=
XM_017005417.1:c.632C=	XP_016860906.1:p.Thr211=
XM_017005419.2:c.779C=	XP_016860908.1:p.Thr260=
XM_017005420.1:c.779C=	XP_016860909.1:p.Thr260=
XM_024453259.1:c.779C=	XP_024309027.1:p.Thr260=