Canonical Allele Identifier: CA1943369383

Gene: C10orf90

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.126579078A= , CM000672.2:g.126579078A=	GRCh38
NC_000010.10:g.128267647A= , CM000672.1:g.128267647A=	GRCh37
NC_000010.9:g.128257637A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000488181.3:c.314-65139T= MANE Select	ENSP00000474558.3:n.314-65139T=
ENST00000488181.2:c.191-65139T=	ENSP00000474558.2:n.191-65139T=
ENST00000657225.1:n.231-65139T=
ENST00000488181.1:c.-119-65139T=	ENSP00000474558.1:n.-119-65139T=
XM_011539216.1:c.314-65139T=	XP_011537518.1:n.314-65139T=
XM_011539219.1:c.-119-65139T=	XP_011537521.1:n.-119-65139T=
XM_011539221.1:c.-119-65139T=	XP_011537523.1:n.-119-65139T=
XM_011539228.1:c.-119-65139T=	XP_011537530.1:n.-119-65139T=
XR_945591.1:n.872-65139T=
NM_001350921.1:c.314-65139T=	NP_001337850.1:n.314-65139T=
NM_001350922.1:c.314-65139T=	NP_001337851.1:n.314-65139T=
NM_001350923.1:c.314-65139T=	NP_001337852.1:n.314-65139T=
NR_146939.1:n.344-65139T=
XR_002956946.1:n.344-65139T=
XR_002956950.1:n.344-65139T=
NM_001350921.2:c.314-65139T= MANE Select	NP_001337850.1:n.314-65139T=
NM_001350922.2:c.314-65139T=	NP_001337851.1:n.314-65139T=
NM_001350923.2:c.314-65139T=	NP_001337852.1:n.314-65139T=
NR_146939.2:n.527-65139T=