Canonical Allele Identifier: CA378567260

Gene: RAB11FIP2

Linked Data

• MyVariant Identifiers: chr10:g.119798754A>T (hg19) ; chr10:g.118039243A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.118039243A>T , CM000672.2:g.118039243A>T	GRCh38
NC_000010.10:g.119798754A>T , CM000672.1:g.119798754A>T	GRCh37
NC_000010.9:g.119788744A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355624.8:c.994T>A MANE Select	ENSP00000347839.3:p.Trp332Arg
ENST00000369199.5:c.994T>A	ENSP00000358200.3:p.Trp332Arg
ENST00000355624.7:c.994T>A	ENSP00000347839.3:p.Trp332Arg
ENST00000369199.4:c.994T>A	ENSP00000358200.3:p.Trp332Arg
ENST00000483413.1:n.388T>A
NM_014904.2:c.994T>A	NP_055719.1:p.Trp332Arg
XM_005269629.2:c.994T>A	XP_005269686.1:p.Trp332Arg
XM_011539511.1:c.994T>A	XP_011537813.1:p.Trp332Arg
XM_011539512.1:c.994T>A	XP_011537814.1:p.Trp332Arg
XM_011539513.1:c.994T>A	XP_011537815.1:p.Trp332Arg
NM_001330167.1:c.994T>A	NP_001317096.1:p.Trp332Arg
XM_017015926.1:c.994T>A	XP_016871415.1:p.Trp332Arg
NM_014904.3:c.994T>A MANE Select	NP_055719.1:p.Trp332Arg
NM_001330167.2:c.994T>A	NP_001317096.1:p.Trp332Arg