Canonical Allele Identifier: CA1943395208

Gene: C10orf90

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.126642144T= , CM000672.2:g.126642144T=	GRCh38
NC_000010.10:g.128330713T= , CM000672.1:g.128330713T=	GRCh37
NC_000010.9:g.128320703T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001350921.2:c.313+4421A= MANE Select	NP_001337850.1:n.313+4421A=
ENST00000488181.3:c.313+4421A= MANE Select	ENSP00000474558.3:n.313+4421A=
NM_001350921.1:c.313+4421A=	NP_001337850.1:n.313+4421A=
NM_001350922.1:c.313+4421A=	NP_001337851.1:n.313+4421A=
NM_001350922.2:c.313+4421A=	NP_001337851.1:n.313+4421A=
NM_001350923.1:c.313+4421A=	NP_001337852.1:n.313+4421A=
NM_001350923.2:c.313+4421A=	NP_001337852.1:n.313+4421A=
NR_146939.1:n.343+4421A=
NR_146939.2:n.526+4421A=
ENST00000488181.1:c.-120+4421A=	ENSP00000474558.1:n.-120+4421A=
ENST00000488181.2:c.190+4421A=	ENSP00000474558.2:n.190+4421A=
ENST00000657225.1:n.230+4421A=
XM_011539216.1:c.313+4421A=	XP_011537518.1:n.313+4421A=
XM_011539219.1:c.-120+4421A=	XP_011537521.1:n.-120+4421A=
XM_011539221.1:c.-120+4421A=	XP_011537523.1:n.-120+4421A=
XM_011539228.1:c.-120+28097A=	XP_011537530.1:n.-120+28097A=
XR_002956946.1:n.343+4421A=
XR_002956950.1:n.343+4421A=
XR_945591.1:n.871+4421A=