Canonical Allele Identifier: CA10318208

Gene: SBF1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50467926G>A , CM000684.2:g.50467926G>A	GRCh38
NC_000022.10:g.50906355G>A , CM000684.1:g.50906355G>A	GRCh37
NC_000022.9:g.49253221G>A	NCBI36
NG_041810.1:g.12146C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348911.11:c.142-3C>T	ENSP00000252027.8:n.142-3C>T
ENST00000399627.4:n.151-3C>T
ENST00000684986.1:c.142-3C>T	ENSP00000509117.1:n.142-3C>T
ENST00000685180.1:n.132-233C>T
ENST00000685809.1:c.142-3C>T	ENSP00000508863.1:n.142-3C>T
ENST00000686222.1:c.142-3C>T	ENSP00000508737.1:n.142-3C>T
ENST00000686427.1:c.142-3C>T	ENSP00000510379.1:n.142-3C>T
ENST00000686801.1:c.142-3C>T	ENSP00000509915.1:n.142-3C>T
ENST00000687016.1:c.142-12C>T	ENSP00000509074.1:n.142-12C>T
ENST00000687340.1:c.169-3C>T	ENSP00000509356.1:n.169-3C>T
ENST00000687704.1:c.142-3C>T	ENSP00000510454.1:n.142-3C>T
ENST00000688066.1:c.130-3C>T	ENSP00000510782.1:n.130-3C>T
ENST00000688124.1:c.142-3C>T	ENSP00000510645.1:n.142-3C>T
ENST00000688848.1:c.142-3C>T	ENSP00000509419.1:n.142-3C>T
ENST00000689129.1:c.142-3C>T	ENSP00000510414.1:n.142-3C>T
ENST00000689981.1:c.142-3C>T	ENSP00000509035.1:n.142-3C>T
ENST00000690155.1:n.328-3C>T
ENST00000690369.1:n.88-3C>T
ENST00000690990.1:c.142-3C>T	ENSP00000510461.1:n.142-3C>T
ENST00000691233.1:c.142-3C>T	ENSP00000509215.1:n.142-3C>T
ENST00000691344.1:c.142-3C>T	ENSP00000509009.1:n.142-3C>T
ENST00000691792.1:c.142-3C>T	ENSP00000509911.1:n.142-3C>T
ENST00000693052.1:c.142-3C>T	ENSP00000509558.1:n.142-3C>T
ENST00000693440.1:c.142-3C>T	ENSP00000509462.1:n.142-3C>T
ENST00000380817.8:c.142-3C>T MANE Select	ENSP00000370196.2:n.142-3C>T
ENST00000348911.10:c.142-3C>T	ENSP00000252027.7:n.142-3C>T
ENST00000380817.7:c.142-3C>T	ENSP00000370196.2:n.142-3C>T
ENST00000399627.3:n.151-3C>T
NM_002972.3:c.142-3C>T	NP_002963.2:n.142-3C>T
XM_005261931.1:c.142-3C>T	XP_005261988.1:n.142-3C>T
XM_005261935.1:c.142-3C>T	XP_005261992.1:n.142-3C>T
XM_011530707.1:c.244-3C>T	XP_011529009.1:n.244-3C>T
XM_011530708.1:c.193-3C>T	XP_011529010.1:n.193-3C>T
XM_011530709.1:c.169-3C>T	XP_011529011.1:n.169-3C>T
XM_011530710.1:c.169-3C>T	XP_011529012.1:n.169-3C>T
XM_011530711.1:c.244-3C>T	XP_011529013.1:n.244-3C>T
XR_938344.1:n.259-3C>T
NM_001365819.1:c.142-3C>T	NP_001352748.1:n.142-3C>T
XM_005261935.2:c.142-3C>T	XP_005261992.1:n.142-3C>T
XM_011530709.2:c.169-3C>T	XP_011529011.1:n.169-3C>T
XM_011530710.2:c.169-3C>T	XP_011529012.1:n.169-3C>T
XM_017028905.2:c.169-3C>T	XP_016884394.1:n.169-3C>T
NM_002972.4:c.142-3C>T MANE Select	NP_002963.2:n.142-3C>T