Canonical Allele Identifier: CA1334204774
Gene: SP110 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.230168722G= , CM000664.2:g.230168722G= GRCh38
NC_000002.11:g.231033438G= , CM000664.1:g.231033438G= GRCh37
NC_000002.10:g.230741682G= NCBI36
NG_008295.1:g.56390C= , LRG_109:g.56390C=

Transcript Alleles

HGVS Amino-acid change
ENST00000698099.1:c.*77+325C= ENSP00000513563.1:n.*77+325C=
ENST00000698100.1:c.*77+325C= ENSP00000513564.1:n.*77+325C=
ENST00000258381.11:c.*402C= MANE Select ENSP00000258381.6:n.*402C=
ENST00000358662.9:c.*402C= ENSP00000351488.4:n.*402C=
ENST00000477068.1:n.1296C=
XM_006712489.2:c.*402C= XP_006712552.1:n.*402C=
XM_005246525.4:c.*402C= XP_005246582.1:n.*402C=
XM_006712489.4:c.*402C= XP_006712552.1:n.*402C=
XM_011511088.3:c.*402C= XP_011509390.1:n.*402C=
XM_011511091.3:c.*402C= XP_011509393.1:n.*402C=
XM_024452850.1:c.*402C= XP_024308618.1:n.*402C=
NM_004509.4:c.*402C= NP_004500.4:n.*402C=
NM_080424.3:c.*402C= NP_536349.3:n.*402C=
NM_001378442.1:c.*402C= NP_001365371.1:n.*402C=
NM_001378443.1:c.*402C= NP_001365372.1:n.*402C=
NM_001378444.1:c.*402C= NP_001365373.1:n.*402C=
NM_001378445.1:c.*402C= NP_001365374.1:n.*402C=
NM_001378446.1:c.*402C= NP_001365375.1:n.*402C=
NM_004509.5:c.*402C= NP_004500.4:n.*402C=
NM_080424.4:c.*402C= MANE Select NP_536349.3:n.*402C=