Canonical Allele Identifier: CA757695971

Gene: SPOPL

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.138521352G>C , CM000664.2:g.138521352G>C	GRCh38
NC_000002.11:g.139278922G>C , CM000664.1:g.139278922G>C	GRCh37
NC_000002.10:g.138995392G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280098.9:c.-61+19233G>C MANE Select	ENSP00000280098.4:n.-61+19233G>C
ENST00000280098.8:c.-61+19233G>C	ENSP00000280098.4:n.-61+19233G>C
ENST00000430968.5:c.-61+19233G>C	ENSP00000410201.1:n.-61+19233G>C
NM_001001664.2:c.-61+19233G>C	NP_001001664.1:n.-61+19233G>C
XM_005263655.3:c.-383+19233G>C	XP_005263712.1:n.-383+19233G>C
XM_005263656.3:c.-312+19233G>C	XP_005263713.1:n.-312+19233G>C
XM_005263657.3:c.-338+19233G>C	XP_005263714.1:n.-338+19233G>C
XM_005263655.5:c.-383+19233G>C	XP_005263712.1:n.-383+19233G>C
XM_005263656.4:c.-312+19233G>C	XP_005263713.1:n.-312+19233G>C
XM_005263657.4:c.-338+19233G>C	XP_005263714.1:n.-338+19233G>C
NM_001001664.3:c.-61+19233G>C MANE Select	NP_001001664.1:n.-61+19233G>C