Canonical Allele Identifier: CA1334204738

Gene: SP110

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.230168638A= , CM000664.2:g.230168638A=	GRCh38
NC_000002.11:g.231033354A= , CM000664.1:g.231033354A=	GRCh37
NC_000002.10:g.230741598A=	NCBI36
NG_008295.1:g.56474T= , LRG_109:g.56474T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698099.1:c.*77+409T=	ENSP00000513563.1:n.*77+409T=
ENST00000698100.1:c.*77+409T=	ENSP00000513564.1:n.*77+409T=
ENST00000258381.11:c.*486T= MANE Select	ENSP00000258381.6:n.*486T=
ENST00000358662.9:c.*486T=	ENSP00000351488.4:n.*486T=
ENST00000477068.1:n.1380T=
XM_006712489.2:c.*486T=	XP_006712552.1:n.*486T=
XM_005246525.4:c.*486T=	XP_005246582.1:n.*486T=
XM_006712489.4:c.*486T=	XP_006712552.1:n.*486T=
XM_011511088.3:c.*486T=	XP_011509390.1:n.*486T=
XM_011511091.3:c.*486T=	XP_011509393.1:n.*486T=
XM_024452850.1:c.*486T=	XP_024308618.1:n.*486T=
NM_004509.4:c.*486T=	NP_004500.4:n.*486T=
NM_080424.3:c.*486T=	NP_536349.3:n.*486T=
NM_001378442.1:c.*486T=	NP_001365371.1:n.*486T=
NM_001378443.1:c.*486T=	NP_001365372.1:n.*486T=
NM_001378444.1:c.*486T=	NP_001365373.1:n.*486T=
NM_001378445.1:c.*486T=	NP_001365374.1:n.*486T=
NM_001378446.1:c.*486T=	NP_001365375.1:n.*486T=
NM_004509.5:c.*486T=	NP_004500.4:n.*486T=
NM_080424.4:c.*486T= MANE Select	NP_536349.3:n.*486T=