Canonical Allele Identifier: CA11101088

Gene: SP110

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.230169808G>T , CM000664.2:g.230169808G>T	GRCh38
NC_000002.11:g.231034524G>T , CM000664.1:g.231034524G>T	GRCh37
NC_000002.10:g.230742768G>T	NCBI36
NG_008295.1:g.55304C>A , LRG_109:g.55304C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698099.1:c.1957-571C>A	ENSP00000513563.1:n.1957-571C>A
ENST00000698100.1:c.1666-571C>A	ENSP00000513564.1:n.1666-571C>A
ENST00000258381.11:c.2029-571C>A MANE Select	ENSP00000258381.6:n.2029-571C>A
ENST00000358662.9:c.1957-571C>A	ENSP00000351488.4:n.1957-571C>A
ENST00000258381.10:c.2029-571C>A	ENSP00000258381.6:n.2029-571C>A
ENST00000358662.8:c.1957-571C>A	ENSP00000351488.4:n.1957-571C>A
ENST00000463022.1:n.296-571C>A
ENST00000477068.1:n.781-571C>A
ENST00000480916.1:n.280-571C>A
ENST00000483067.1:n.248-571C>A
NM_004509.3:c.1957-571C>A	NP_004500.3:n.1957-571C>A
NM_080424.2:c.2029-571C>A , LRG_109t1:c.2029-571C>A	NP_536349.2:n.2029-571C>A
XM_005246525.2:c.2047-571C>A	XP_005246582.1:n.2047-571C>A
XM_006712487.2:c.1975-571C>A	XP_006712550.1:n.1975-571C>A
XM_006712489.2:c.1834-571C>A	XP_006712552.1:n.1834-571C>A
XM_011511088.1:c.2125-571C>A	XP_011509390.1:n.2125-571C>A
XM_011511089.1:c.2107-571C>A	XP_011509391.1:n.2107-571C>A
XM_011511090.1:c.1975-571C>A	XP_011509392.1:n.1975-571C>A
XM_011511091.1:c.1906-571C>A	XP_011509393.1:n.1906-571C>A
XM_011511092.1:c.1498-571C>A	XP_011509394.1:n.1498-571C>A
XM_005246525.4:c.2047-571C>A	XP_005246582.1:n.2047-571C>A
XM_006712487.3:c.1975-571C>A	XP_006712550.1:n.1975-571C>A
XM_006712489.4:c.1834-571C>A	XP_006712552.1:n.1834-571C>A
XM_011511088.3:c.2125-571C>A	XP_011509390.1:n.2125-571C>A
XM_011511089.3:c.2107-571C>A	XP_011509391.1:n.2107-571C>A
XM_011511090.3:c.1975-571C>A	XP_011509392.1:n.1975-571C>A
XM_011511091.3:c.1906-571C>A	XP_011509393.1:n.1906-571C>A
XM_011511092.3:c.1498-571C>A	XP_011509394.1:n.1498-571C>A
XM_017003968.2:c.2125-571C>A	XP_016859457.1:n.2125-571C>A
XM_024452850.1:c.1684-571C>A	XP_024308618.1:n.1684-571C>A
NM_004509.4:c.1957-571C>A	NP_004500.4:n.1957-571C>A
NM_080424.3:c.2029-571C>A	NP_536349.3:n.2029-571C>A
NM_001378442.1:c.2125-571C>A	NP_001365371.1:n.2125-571C>A
NM_001378443.1:c.2107-571C>A	NP_001365372.1:n.2107-571C>A
NM_001378444.1:c.2047-571C>A	NP_001365373.1:n.2047-571C>A
NM_001378445.1:c.1975-571C>A	NP_001365374.1:n.1975-571C>A
NM_001378446.1:c.1834-571C>A	NP_001365375.1:n.1834-571C>A
NM_004509.5:c.1957-571C>A	NP_004500.4:n.1957-571C>A
NM_080424.4:c.2029-571C>A MANE Select	NP_536349.3:n.2029-571C>A