Canonical Allele Identifier: CA10317057

Gene: SBF1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50461577C>T , CM000684.2:g.50461577C>T	GRCh38
NC_000022.10:g.50900006C>T , CM000684.1:g.50900006C>T	GRCh37
NC_000022.9:g.49246872C>T	NCBI36
NG_041810.1:g.18495G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348911.11:c.2785G>A	ENSP00000252027.8:p.Val929Ile
ENST00000684986.1:c.2788G>A	ENSP00000509117.1:p.Val930Ile
ENST00000685180.1:n.2309+370G>A
ENST00000685386.1:c.655G>A	ENSP00000510338.1:p.Val219Ile
ENST00000685390.1:n.1028G>A
ENST00000685809.1:c.2776G>A	ENSP00000508863.1:p.Val926Ile
ENST00000686222.1:c.*2207G>A	ENSP00000508737.1:n.*2207G>A
ENST00000686427.1:c.2785G>A	ENSP00000510379.1:p.Val929Ile
ENST00000686801.1:c.2773G>A	ENSP00000509915.1:p.Val925Ile
ENST00000687016.1:c.2764G>A	ENSP00000509074.1:p.Val922Ile
ENST00000687704.1:c.*599G>A	ENSP00000510454.1:n.*599G>A
ENST00000688030.1:c.594G>A	ENSP00000508668.1:p.Pro198=
ENST00000688066.1:c.2785G>A	ENSP00000510782.1:p.Val929Ile
ENST00000688124.1:c.*1779G>A	ENSP00000510645.1:n.*1779G>A
ENST00000688848.1:c.*2207G>A	ENSP00000509419.1:n.*2207G>A
ENST00000689129.1:c.2788G>A	ENSP00000510414.1:p.Val930Ile
ENST00000689177.1:n.636G>A
ENST00000689981.1:c.2785G>A	ENSP00000509035.1:p.Val929Ile
ENST00000690369.1:n.2803G>A
ENST00000690990.1:c.2779G>A	ENSP00000510461.1:p.Val927Ile
ENST00000691233.1:c.2782G>A	ENSP00000509215.1:p.Val928Ile
ENST00000691345.1:n.1286G>A
ENST00000691792.1:c.2785G>A	ENSP00000509911.1:p.Val929Ile
ENST00000691959.1:n.2664G>A
ENST00000693052.1:c.2785G>A	ENSP00000509558.1:p.Val929Ile
ENST00000693440.1:c.2782G>A	ENSP00000509462.1:p.Val928Ile
ENST00000693499.1:n.2430G>A
ENST00000380817.8:c.2785G>A MANE Select	ENSP00000370196.2:p.Val929Ile
ENST00000348911.10:c.2788G>A	ENSP00000252027.7:p.Val930Ile
ENST00000380817.7:c.2785G>A	ENSP00000370196.2:p.Val929Ile
NM_002972.3:c.2785G>A	NP_002963.2:p.Val929Ile
XM_005261931.1:c.2788G>A	XP_005261988.1:p.Val930Ile
XM_005261935.1:c.2785G>A	XP_005261992.1:p.Val929Ile
XM_011530707.1:c.2887G>A	XP_011529009.1:p.Val963Ile
XM_011530708.1:c.2839G>A	XP_011529010.1:p.Val947Ile
XM_011530709.1:c.2815G>A	XP_011529011.1:p.Val939Ile
XM_011530710.1:c.2812G>A	XP_011529012.1:p.Val938Ile
XM_011530711.1:c.2890G>A	XP_011529013.1:p.Val964Ile
XR_938344.1:n.2905G>A
NM_001365819.1:c.2788G>A	NP_001352748.1:p.Val930Ile
XM_005261935.2:c.2785G>A	XP_005261992.1:p.Val929Ile
XM_011530709.2:c.2815G>A	XP_011529011.1:p.Val939Ile
XM_011530710.2:c.2812G>A	XP_011529012.1:p.Val938Ile
XM_017028905.2:c.2815G>A	XP_016884394.1:p.Val939Ile
NM_002972.4:c.2785G>A MANE Select	NP_002963.2:p.Val929Ile